11-33772170-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33772170
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33772170
    reference: chr 11
allele count: 1
allele frequency: 8.261731658955718e-6
allele num: 121040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.832G>A
  hgvsp: ENSP00000433781.1:p.Asp278Asn
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.508G>A
  hgvsp: ENSP00000435680.1:p.Asp170Asn
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.847G>A
  hgvsp: ENSP00000265651.3:p.Asp283Asn
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*123G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2219G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.847G>A
  hgvsp: ENSP00000408836.2:p.Asp283Asn
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.847G>A
  hgvsp: ENSP00000431745.1:p.Asp283Asn
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-93G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-93G>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25889
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7649
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp283Asn
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

11-33772170-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33772170
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33772170
    reference: chr 11
allele count: 1
allele frequency: 8.261731658955718e-6
allele num: 121040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.847G>C
  hgvsp: ENSP00000408836.2:p.Asp283His
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*123G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2219G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.508G>C
  hgvsp: ENSP00000435680.1:p.Asp170His
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-93G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.847G>C
  hgvsp: ENSP00000431745.1:p.Asp283His
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.832G>C
  hgvsp: ENSP00000433781.1:p.Asp278His
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.847G>C
  hgvsp: ENSP00000265651.3:p.Asp283His
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-93G>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp283His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/11-33772171-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33772171
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33772171
    reference: chr 11
allele count: 1
allele frequency: 8.262414277451872e-6
allele num: 121030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2218G>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.831G>T
  hgvsp: ENST00000530401.1:c.831G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-94G>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.846G>T
  hgvsp: ENST00000448981.2:c.846G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*122G>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.846G>T
  hgvsp: ENST00000265651.3:c.846G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.507G>T
  hgvsp: ENST00000526785.1:c.507G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.846G>T
  hgvsp: ENST00000534136.1:c.846G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-94G>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly282Gly
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

11-33772171-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33772171
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33772171
    reference: chr 11
allele count: 2
allele frequency: 1.652482855490374e-5
allele num: 121030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-94G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.846G>A
  hgvsp: ENST00000448981.2:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.507G>A
  hgvsp: ENST00000526785.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.831G>A
  hgvsp: ENST00000530401.1:c.831G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.846G>A
  hgvsp: ENST00000265651.3:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-94G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.846G>A
  hgvsp: ENST00000534136.1:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*122G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2218G>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18289
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25907
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41260
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly282Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum

11-33772175-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33772175
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33772175
    reference: chr 11
allele count: 1
allele frequency: 8.263916435277007e-6
allele num: 121008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.503C>T
  hgvsp: ENSP00000435680.1:p.Thr168Ile
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2214C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.842C>T
  hgvsp: ENSP00000265651.3:p.Thr281Ile
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-98C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.827C>T
  hgvsp: ENSP00000433781.1:p.Thr276Ile
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.842C>T
  hgvsp: ENSP00000408836.2:p.Thr281Ile
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-98C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.842C>T
  hgvsp: ENSP00000431745.1:p.Thr281Ile
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*118C>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41291
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr281Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-33772176-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33772176
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33772176
    reference: chr 11
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.841A>G
  hgvsp: ENSP00000408836.2:p.Thr281Ala
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.841A>G
  hgvsp: ENSP00000265651.3:p.Thr281Ala
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-99A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.826A>G
  hgvsp: ENSP00000433781.1:p.Thr276Ala
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*117A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2213A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.502A>G
  hgvsp: ENSP00000435680.1:p.Thr168Ala
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.841A>G
  hgvsp: ENSP00000431745.1:p.Thr281Ala
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-99A>G
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr281Ala
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

11-33772191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33772191
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33772191
    reference: chr 11
allele count: 4
allele frequency: 3.311806590495115e-5
allele num: 120780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.826G>A
  hgvsp: ENSP00000408836.2:p.Glu276Lys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.487G>A
  hgvsp: ENSP00000435680.1:p.Glu163Lys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.826G>A
  hgvsp: ENSP00000265651.3:p.Glu276Lys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-114G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.811G>A
  hgvsp: ENSP00000433781.1:p.Glu271Lys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-114G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.826G>A
  hgvsp: ENSP00000431745.1:p.Glu276Lys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2198G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*102G>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25945
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7588
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu276Lys
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

11-33772197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33772197
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33772197
    reference: chr 11
allele count: 2
allele frequency: 1.658814942605003e-5
allele num: 120568
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*96G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.820G>A
  hgvsp: ENSP00000265651.3:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.820G>A
  hgvsp: ENSP00000408836.2:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-120G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2192G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.481G>A
  hgvsp: ENSP00000435680.1:p.Asp161Asn
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-120G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.805G>A
  hgvsp: ENSP00000433781.1:p.Asp269Asn
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.820G>A
  hgvsp: ENSP00000431745.1:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8581
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2204
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp274Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-33772227-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33772227
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33772227
    reference: chr 11
allele count: 1
allele frequency: 8.53373384990869e-6
allele num: 117182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.810-20T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.810-20T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.795-20T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-130-20T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.810-20T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*86-20T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.471-20T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2182-20T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-130-20T>G
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8041
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3137
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

11-33772237-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33772237
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33772237
    reference: chr 11
allele count: 1
allele frequency: 8.582954252853832e-6
allele num: 116510
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-130-30T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*86-30T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-130-30T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.810-30T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.795-30T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.810-30T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2182-30T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.471-30T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.810-30T>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8716
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15735
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22761
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2984
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

11-33773031-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773031
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773031
    reference: chr 11
allele count: 105
allele frequency: 9.147935180345008e-4
allele num: 114780
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.809+38T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-131+38T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.794+38T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-131+38T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.470+38T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2181+38T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*85+38T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.809+38T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.809+38T>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8850
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4887
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19559
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3263
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3473
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5065
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3298
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

11-33773050-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773050
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773050
    reference: chr 11
allele count: 1
allele frequency: 8.510638297872341e-6
allele num: 117500
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2181+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.809+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-131+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.470+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.809+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.809+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-131+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*85+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.794+19T>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10917
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/11-33773060-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773060
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773060
    reference: chr 11
allele count: 1
allele frequency: 8.400678774845007e-6
allele num: 119038
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.809+9T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-131+9T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.470+9T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2181+9T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-131+9T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*85+9T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.809+9T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.809+9T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.794+9T>G
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28410
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum

11-33773061-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773061
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773061
    reference: chr 11
allele count: 2
allele frequency: 1.67895099142056e-5
allele num: 119122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.470+8A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2181+8A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-131+8A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.794+8A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.809+8A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-131+8A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*85+8A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.809+8A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.809+8A>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6248
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28501
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6471
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
hgvs: c.809+8A>C
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

11-33773077-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773077
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773077
    reference: chr 11
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-139A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.801A>G
  hgvsp: ENST00000534136.1:c.801A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.786A>G
  hgvsp: ENST00000530401.1:c.786A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.801A>G
  hgvsp: ENST00000448981.2:c.801A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-139A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.801A>G
  hgvsp: ENST00000265651.3:c.801A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.462A>G
  hgvsp: ENST00000526785.1:c.462A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2173A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*77A>G
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12105
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2763
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln267Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

11-33773077-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773077
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773077
    reference: chr 11
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-139A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.801A>C
  hgvsp: ENSP00000431745.1:p.Gln267His
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.462A>C
  hgvsp: ENSP00000435680.1:p.Gln154His
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*77A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.801A>C
  hgvsp: ENSP00000265651.3:p.Gln267His
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.801A>C
  hgvsp: ENSP00000408836.2:p.Gln267His
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-139A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.786A>C
  hgvsp: ENSP00000433781.1:p.Gln262His
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2173A>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2763
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gln267His
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-33773089-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773089
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773089
    reference: chr 11
allele count: 1
allele frequency: 8.291461452995706e-6
allele num: 120606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.789C>T
  hgvsp: ENST00000448981.2:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.789C>T
  hgvsp: ENST00000265651.3:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*65C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.789C>T
  hgvsp: ENST00000534136.1:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.774C>T
  hgvsp: ENST00000530401.1:c.774C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-151C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-151C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2161C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.450C>T
  hgvsp: ENST00000526785.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1734
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3845
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile263Ile
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

11-33773091-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773091
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773091
    reference: chr 11
allele count: 13
allele frequency: 1.077550479095521e-4
allele num: 120644
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.787A>C
  hgvsp: ENSP00000431745.1:p.Ile263Leu
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.787A>C
  hgvsp: ENSP00000265651.3:p.Ile263Leu
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.787A>C
  hgvsp: ENSP00000408836.2:p.Ile263Leu
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.772A>C
  hgvsp: ENSP00000433781.1:p.Ile258Leu
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.448A>C
  hgvsp: ENSP00000435680.1:p.Ile150Leu
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-153A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-153A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2159A>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*63A>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2783
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2934
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29823
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile263Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

11-33773093-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773093
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773093
    reference: chr 11
allele count: 1
allele frequency: 8.287201246395068e-6
allele num: 120668
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.785C>G
  hgvsp: ENSP00000265651.3:p.Pro262Arg
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-155C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.770C>G
  hgvsp: ENSP00000433781.1:p.Pro257Arg
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*61C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-155C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.785C>G
  hgvsp: ENSP00000431745.1:p.Pro262Arg
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.446C>G
  hgvsp: ENSP00000435680.1:p.Pro149Arg
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.785C>G
  hgvsp: ENSP00000408836.2:p.Pro262Arg
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2157C>G
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro262Arg
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

11-33773104-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773104
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773104
    reference: chr 11
allele count: 2
allele frequency: 1.656012983141788e-5
allele num: 120772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-166A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2146A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.774A>G
  hgvsp: ENST00000265651.3:c.774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.774A>G
  hgvsp: ENST00000448981.2:c.774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.435A>G
  hgvsp: ENST00000526785.1:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.774A>G
  hgvsp: ENST00000534136.1:c.774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-166A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.759A>G
  hgvsp: ENST00000530401.1:c.759A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29833
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser258Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-33773113-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773113
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773113
    reference: chr 11
allele count: 1
allele frequency: 8.276638360563474e-6
allele num: 120822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-175T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.750T>G
  hgvsp: ENSP00000433781.1:p.Asn250Lys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.765T>G
  hgvsp: ENSP00000431745.1:p.Asn255Lys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2137T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.426T>G
  hgvsp: ENSP00000435680.1:p.Asn142Lys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.765T>G
  hgvsp: ENSP00000265651.3:p.Asn255Lys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-175T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.765T>G
  hgvsp: ENSP00000408836.2:p.Asn255Lys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*41T>G
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1732
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn255Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

11-33773117-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773117
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773117
    reference: chr 11
allele count: 1
allele frequency: 8.275953389830508e-6
allele num: 120832
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-179A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*37A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.746A>G
  hgvsp: ENSP00000433781.1:p.Lys249Arg
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2133A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.761A>G
  hgvsp: ENSP00000431745.1:p.Lys254Arg
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.761A>G
  hgvsp: ENSP00000408836.2:p.Lys254Arg
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-179A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.761A>G
  hgvsp: ENSP00000265651.3:p.Lys254Arg
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.422A>G
  hgvsp: ENSP00000435680.1:p.Lys141Arg
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys254Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

11-33773119-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773119
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773119
    reference: chr 11
allele count: 1
allele frequency: 8.276090374906894e-6
allele num: 120830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-181C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.759C>T
  hgvsp: ENST00000534136.1:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2131C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.420C>T
  hgvsp: ENST00000526785.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.759C>T
  hgvsp: ENST00000448981.2:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.744C>T
  hgvsp: ENST00000530401.1:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*35C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.759C>T
  hgvsp: ENST00000265651.3:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-181C>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3853
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val253Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

11-33773130-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773130
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773130
    reference: chr 11
allele count: 1
allele frequency: 8.275131574592036e-6
allele num: 120844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.748A>T
  hgvsp: ENSP00000431745.1:p.Thr250Ser
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.409A>T
  hgvsp: ENSP00000435680.1:p.Thr137Ser
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.733A>T
  hgvsp: ENSP00000433781.1:p.Thr245Ser
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-192A>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-192A>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2120A>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*24A>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.748A>T
  hgvsp: ENSP00000265651.3:p.Thr250Ser
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.748A>T
  hgvsp: ENSP00000408836.2:p.Thr250Ser
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29532
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr250Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ

11-33773161-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773161
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773161
    reference: chr 11
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-8C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-8C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-8C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-8C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-8C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-8C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-8C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-8C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-8C>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
hgvs: c.725-8C>T
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

11-33773161-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773161
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773161
    reference: chr 11
allele count: 119832
allele frequency: 9.906909836472164e-1
allele num: 120958
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-8C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-8C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-8C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-8C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-8C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-8C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-8C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-8C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-8C>G
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.75e1
  variant carriers: 1475
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 2.25e1
  variant carriers: 2769
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 3.25e1
  variant carriers: 6511
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 6.25e1
  variant carriers: 3367
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 8.75e1
  variant carriers: 800
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 1.75e1
  variant carriers: 1280
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 8.25e1
  variant carriers: 1067
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 5.75e1
  variant carriers: 4342
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 2.75e1
  variant carriers: 4838
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 9.25e1
  variant carriers: 560
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 3.75e1
  variant carriers: 7339
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 164
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.25e1
  variant carriers: 533
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 7.25e1
  variant carriers: 1799
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 4.25e1
  variant carriers: 7267
genotype depth: GenotypeDepth
  all individuals: 6386
  bin: 4.75e1
  variant carriers: 6386
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 5.25e1
  variant carriers: 5341
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 9.75e1
  variant carriers: 2311
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 6.75e1
  variant carriers: 2455
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 85
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.25e1
  variant carriers: 153
hgvs: c.725-8C>G
num of homozygotes: 59397
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

11-33773173-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773173
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773173
    reference: chr 11
allele count: 7
allele frequency: 6.127987393854505e-5
allele num: 114230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-20C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-20C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-20C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-20C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-20C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-20C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-20C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-20C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-20C>G
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28129
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5781
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

11-33773173-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773173
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773174
    reference: chr 11
allele count: 3
allele frequency: 2.62628031165193e-5
allele num: 114230
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-21dupT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-21dupT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-21dupT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-21dupT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-21dupT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-21dupT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-21dupT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-21dupT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-21dupT
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11235
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5781
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

11-33773180-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773180
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773180
    reference: chr 11
allele count: 1
allele frequency: 8.826281134706703e-6
allele num: 113298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-27T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-27T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-27T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-27T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-27T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-27T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-27T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-27T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-27T>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4417
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3347
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

11-33773181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773181
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773181
    reference: chr 11
allele count: 3
allele frequency: 2.657783762713066e-5
allele num: 112876
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-28C>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-33773181-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773181
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773180
    reference: chr 11
allele count: 1
allele frequency: 8.859279209043553e-6
allele num: 112876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-29delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-29delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-29delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-29delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-29delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-29delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-29delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-29delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-29delT
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17376
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24287
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2321
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: GA
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-33773181-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773181
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773181
    reference: chr 11
allele count: 1
allele frequency: 8.859279209043553e-6
allele num: 112876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-28C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-28C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-28C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-28C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-28C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-28C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-28C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-28C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-28C>G
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3342
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4394
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

11-33773186-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773186
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773186
    reference: chr 11
allele count: 36
allele frequency: 3.226268999139662e-4
allele num: 111584
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-33C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-33C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-33C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-33C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-33C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-33C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-33C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-33C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-33C>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13984
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7008
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15927
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9206
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3757
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 9.75e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 19164
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3643
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

11-33773189-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773189
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773189
    reference: chr 11
allele count: 2
allele frequency: 1.813960237991583e-5
allele num: 110256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-36G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-36G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-36G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-36G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-36G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-36G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-36G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-36G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-36G>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11655
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2742
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13050
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1324
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4458
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-33773192-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773192
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773192
    reference: chr 11
allele count: 2
allele frequency: 1.829692245764263e-5
allele num: 109308
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-39T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-39T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-39T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-39T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-39T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-39T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-39T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-39T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-39T>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15099
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2091
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7701
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12661
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2741
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

11-33773200-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33773200
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33773200
    reference: chr 11
allele count: 8
allele frequency: 7.65579543714592e-5
allele num: 104496
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.710-47C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.725-47C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435165
  ensembl transcript: ENST00000531080
  gene symbol: FBXO3
  hgvsc: ENST00000531080.1:c.-215-47C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*1-47C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434001
  ensembl transcript: ENST00000532057
  gene symbol: FBXO3
  hgvsc: ENST00000532057.1:c.-215-47C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.386-47C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.725-47C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.725-47C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.2097-47C>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15290
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8762
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15493
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1838
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10858
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7130
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

11-33775955-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775955
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775955
    reference: chr 11
allele count: 7
allele frequency: 6.204793646291306e-5
allele num: 112816
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.798A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*46A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+46A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+46A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+46A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+46A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+46A>G
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10218
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3699
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4730
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3666
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4015
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16246
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1550
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

11-33775959-G-GGAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775959
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775962
    reference: chr 11
allele count: 1
allele frequency: 9.00835975785529e-6
allele num: 111008
alternate allele: GGAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.791_793dupTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+39_724+41dupTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*39_*41dupTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+39_724+41dupTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+39_385+41dupTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+39_724+41dupTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+39_709+41dupTTC
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7334
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1732
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

11-33775959-GGAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775959
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775956
    reference: chr 11
allele count: 24
allele frequency: 2.162006341885269e-4
allele num: 111008
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+39_724+41delTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.791_793delTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+39_385+41delTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+39_709+41delTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+39_724+41delTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*39_*41delTTC
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+39_724+41delTTC
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9432
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21030
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 19372
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3742
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3762
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1874
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 7.5e0
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: GGAA
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

11-33775974-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775974
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775974
    reference: chr 11
allele count: 1
allele frequency: 8.61000137760022e-6
allele num: 116144
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+27C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*27C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.779C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+27C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+27C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+27C>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+27C>G
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11426
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3268
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27623
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

11-33775975-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775975
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775975
    reference: chr 11
allele count: 1
allele frequency: 8.592837011067574e-6
allele num: 116376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+26C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*26C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+26C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+26C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.778C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+26C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+26C>T
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2531
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6794
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7623
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1379
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2400
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27910
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-33775976-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775976
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775975
    reference: chr 11
allele count: 1
allele frequency: 8.581186606483944e-6
allele num: 116534
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+24delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+24delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.776delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*24delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+24delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+24delT
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+24delT
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1317
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3300
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2613
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: GA
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

11-33775977-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775977
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775977
    reference: chr 11
allele count: 1
allele frequency: 8.561643835616438e-6
allele num: 116800
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+24T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+24T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+24T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+24T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+24T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.776T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*24T>C
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2642
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3336
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2191
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

11-33775978-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775978
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775978
    reference: chr 11
allele count: 1
allele frequency: 8.539855505644844e-6
allele num: 117098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+23T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*23T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+23T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+23T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+23T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.775T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+23T>C
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2598
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2062
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6978
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

11-33775982-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775982
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775982
    reference: chr 11
allele count: 45740
allele frequency: 3.83049995812746e-1
allele num: 119410
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+19T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.771T>C
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 6.25e1
  variant carriers: 1263
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 3.75e1
  variant carriers: 4981
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 414
genotype depth: GenotypeDepth
  all individuals: 7799
  bin: 3.25e1
  variant carriers: 5140
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 534
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.5e0
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.25e1
  variant carriers: 422
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.75e1
  variant carriers: 1766
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.25e1
  variant carriers: 2503
genotype depth: GenotypeDepth
  all individuals: 14042
  bin: 2.25e1
  variant carriers: 2991
genotype depth: GenotypeDepth
  all individuals: 10343
  bin: 2.75e1
  variant carriers: 4549
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.25e1
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 4.75e1
  variant carriers: 3318
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 1.75e1
  variant carriers: 1474
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 6.75e1
  variant carriers: 826
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 228
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 9.75e1
  variant carriers: 1768
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 4.25e1
  variant carriers: 4348
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 8.25e1
  variant carriers: 275
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 7.25e1
  variant carriers: 216
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
  variant carriers: 148
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.5e0
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 8.75e1
  variant carriers: 278
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.75e1
  variant carriers: 93
genotype quality: GenotypeQuality
  all individuals: 3184
  bin: 6.75e1
  variant carriers: 368
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 8.25e1
  variant carriers: 465
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.5e0
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.75e1
  variant carriers: 141
num of homozygotes: 8835
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-33775984-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775984
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775984
    reference: chr 11
allele count: 1
allele frequency: 8.337085021593051e-6
allele num: 119946
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+17T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+17T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.769T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+17T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+17T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+17T>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*17T>G
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9308
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6439
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

11-33775986-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775986
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775986
    reference: chr 11
allele count: 5
allele frequency: 4.164584374479427e-5
allele num: 120060
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+15A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.767A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+15A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+15A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+15A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*15A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+15A>G
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20689
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16552
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9313
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3175
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP

11-33775993-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775993
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775993
    reference: chr 11
allele count: 1
allele frequency: 8.309650828472188e-6
allele num: 120342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+8A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+8A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.760A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+8A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+8A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*8A>G
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+8A>G
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1906
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 3.75e1
  variant carriers: 0
hgvs: c.724+8A>G
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS

11-33775997-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33775997
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33775997
    reference: chr 11
allele count: 155
allele frequency: 1.286307053941909e-3
allele num: 120500
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.724+4G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.*4G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.385+4G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.724+4G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.756G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.724+4G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.709+4G>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 5.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 17584
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10533
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 20992
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6474
  bin: 9.75e1
  variant carriers: 153
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.75e1
  variant carriers: 1
hgvs: c.724+4G>C
num of homozygotes: 1
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

11-33776003-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33776003
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33776003
    reference: chr 11
allele count: 1
allele frequency: 8.288712431410904e-6
allele num: 120646
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.750T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.722T>C
  hgvsp: ENSP00000431745.1:p.Ile241Thr
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.722T>C
  hgvsp: ENSP00000265651.3:p.Ile241Thr
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.722T>C
  hgvsp: ENSP00000408836.2:p.Ile241Thr
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.383T>C
  hgvsp: ENSP00000435680.1:p.Ile128Thr
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.517T>C
  hgvsp: ENSP00000434099.1:p.Ter173GlnextTer37
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.707T>C
  hgvsp: ENSP00000433781.1:p.Ile236Thr
  variant of: http://identifiers.org/hgnc/13582
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9379
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34207
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ter173GlnextTer37
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

11-33776004-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33776004
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33776004
    reference: chr 11
allele count: 4
allele frequency: 3.315045333244932e-5
allele num: 120662
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.382A>G
  hgvsp: ENSP00000435680.1:p.Ile128Val
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.516A>G
  hgvsp: ENST00000532927.1:c.516A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.706A>G
  hgvsp: ENSP00000433781.1:p.Ile236Val
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.721A>G
  hgvsp: ENSP00000431745.1:p.Ile241Val
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.721A>G
  hgvsp: ENSP00000265651.3:p.Ile241Val
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.721A>G
  hgvsp: ENSP00000408836.2:p.Ile241Val
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.749A>G
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2612
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6348
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 9387
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile241Val
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

11-33776033-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33776033
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33776033
    reference: chr 11
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.692G>A
  hgvsp: ENSP00000408836.2:p.Arg231Gln
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.353G>A
  hgvsp: ENSP00000435680.1:p.Arg118Gln
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.677G>A
  hgvsp: ENSP00000433781.1:p.Arg226Gln
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.692G>A
  hgvsp: ENSP00000265651.3:p.Arg231Gln
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.487G>A
  hgvsp: ENSP00000434099.1:p.Glu163Lys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.720G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.692G>A
  hgvsp: ENSP00000431745.1:p.Arg231Gln
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34534
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9362
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2617
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg231Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/11-33776037-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33776037
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33776037
    reference: chr 11
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.349G>T
  hgvsp: ENSP00000435680.1:p.Ala117Ser
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.688G>T
  hgvsp: ENSP00000431745.1:p.Ala230Ser
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.483G>T
  hgvsp: ENSP00000434099.1:p.Trp161Cys
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.673G>T
  hgvsp: ENSP00000433781.1:p.Ala225Ser
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.688G>T
  hgvsp: ENSP00000408836.2:p.Ala230Ser
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.688G>T
  hgvsp: ENSP00000265651.3:p.Ala230Ser
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.716G>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6337
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34483
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala230Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

11-33776049-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33776049
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33776049
    reference: chr 11
allele count: 4
allele frequency: 3.31746479340488e-5
allele num: 120574
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.679-3T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.340-3T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.664-3T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-3T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.679-3T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.679-3T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.707-3T>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6336
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3053
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
hgvs: c.679-3T>C
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

11-33776053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33776053
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33776053
    reference: chr 11
allele count: 1
allele frequency: 8.298617450332775e-6
allele num: 120502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.664-7C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.679-7C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.340-7C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.679-7C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.707-7C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.679-7C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-7C>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3026
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6332
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 2.75e1
  variant carriers: 0
hgvs: c.679-7C>T
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-33776066-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33776066
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33776066
    reference: chr 11
allele count: 1
allele frequency: 8.325008325008325e-6
allele num: 120120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.679-20G>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.707-20G>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.664-20G>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-20G>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.340-20G>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.679-20G>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.679-20G>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10305
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1837
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30896
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2455
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-33776070-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33776070
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33776070
    reference: chr 11
allele count: 1
allele frequency: 8.334027835652971e-6
allele num: 119990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.340-24G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.707-24G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-24G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.664-24G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.679-24G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.679-24G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.679-24G>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10020
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2933
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29505
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8469
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

11-33776071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33776071
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33776071
    reference: chr 11
allele count: 4
allele frequency: 3.33438922325403e-5
allele num: 119962
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.679-25C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.664-25C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.679-25C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-25C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.340-25C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.679-25C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.707-25C>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19753
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13946
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8421
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29084
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6344
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-33776071-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33776071
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33776071
    reference: chr 11
allele count: 33
allele frequency: 2.750871109184575e-4
allele num: 119962
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.664-25C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-25C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.679-25C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.679-25C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.340-25C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.679-25C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.707-25C>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19753
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13946
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9856
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 983
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2506
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

11-33776081-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33776081
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33776081
    reference: chr 11
allele count: 2
allele frequency: 1.672492515595993e-5
allele num: 119582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.340-35G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.679-35G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.679-35G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.664-35G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.707-35G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.679-35G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-35G>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5653
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3523
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1906
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-33777267-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33777267
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33777267
    reference: chr 11
allele count: 16
allele frequency: 1.334623469353709e-4
allele num: 119884
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-1221T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.339+50T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.678+50T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.678+50T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.678+50T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.663+50T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.706+50T>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19069
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8157
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16466
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2756
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3933
  bin: 9.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6679
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

11-33777276-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33777276
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33777276
    reference: chr 11
allele count: 1
allele frequency: 8.330278897737497e-6
allele num: 120044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.678+41T>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.678+41T>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.706+41T>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.339+41T>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.663+41T>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.678+41T>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-1230T>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20475
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2149
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ

11-33777278-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33777278
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33777278
    reference: chr 11
allele count: 1
allele frequency: 8.332638946754437e-6
allele num: 120010
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.678+39G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.678+39G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.678+39G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.706+39G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-1232G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.339+39G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.663+39G>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6887
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20079
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1741
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34415
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2528
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

11-33777288-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33777288
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33777288
    reference: chr 11
allele count: 1
allele frequency: 8.311170212765958e-6
allele num: 120320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.663+29A>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.678+29A>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-1242A>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.678+29A>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.678+29A>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.339+29A>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.706+29A>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20819
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38226
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2174
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

11-33777289-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33777289
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33777289
    reference: chr 11
allele count: 5
allele frequency: 4.1556541830815e-5
allele num: 120318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.339+28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-1243C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.678+28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.663+28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.678+28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.706+28C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.678+28C>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7118
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20941
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6871
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2568
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

11-33777300-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33777300
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33777300
    reference: chr 11
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: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-1254T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.663+17T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.678+17T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.678+17T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.706+17T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.678+17T>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.339+17T>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7205
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3930
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

11-33777301-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33777301
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33777301
    reference: chr 11
allele count: 1
allele frequency: 8.281710670156027e-6
allele num: 120748
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.678+16G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.706+16G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-1255G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.663+16G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.339+16G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.678+16G>C
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.678+16G>C
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3929
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum

11-33777305-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33777305
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33777305
    reference: chr 11
allele count: 2
allele frequency: 1.654916757687088e-5
allele num: 120852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.706+12G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-1259G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.678+12G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.678+12G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.678+12G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.663+12G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.339+12G>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1821
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7044
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2641
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

11-33777306-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33777306
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33777306
    reference: chr 11
allele count: 162
allele frequency: 1.340083382966051e-3
allele num: 120888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.706+11C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.339+11C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.678+11C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.663+11C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.678+11C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.678+11C>T
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-1260C>T
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21836
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 24550
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2635
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2202
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

11-33777306-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33777306
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33777306
    reference: chr 11
allele count: 1
allele frequency: 8.272119647938589e-6
allele num: 120888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.706+11C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.678+11C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.678+11C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.339+11C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-1260C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.678+11C>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.663+11C>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2635
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-33777334-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33777334
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 33777334
    reference: chr 11
allele count: 8024
allele frequency: 6.618932919787508e-2
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000433781
  ensembl transcript: ENST00000530401
  gene symbol: FBXO3
  hgvsc: ENST00000530401.1:c.646G>A
  hgvsp: ENSP00000433781.1:p.Val216Ile
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000265651
  ensembl transcript: ENST00000265651
  gene symbol: FBXO3
  hgvsc: ENST00000265651.3:c.661G>A
  hgvsp: ENSP00000265651.3:p.Val221Ile
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000435680
  ensembl transcript: ENST00000526785
  gene symbol: FBXO3
  hgvsc: ENST00000526785.1:c.322G>A
  hgvsp: ENSP00000435680.1:p.Val108Ile
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110429
  ensembl transcript: ENST00000530013
  gene symbol: FBXO3
  hgvsc: ENST00000530013.1:n.689G>A
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000408836
  ensembl transcript: ENST00000448981
  gene symbol: FBXO3
  hgvsc: ENST00000448981.2:c.661G>A
  hgvsp: ENSP00000408836.2:p.Val221Ile
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000431745
  ensembl transcript: ENST00000534136
  gene symbol: FBXO3
  hgvsc: ENST00000534136.1:c.661G>A
  hgvsp: ENSP00000431745.1:p.Val221Ile
  variant of: http://identifiers.org/hgnc/13582
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110429
  ensembl protein: ENSP00000434099
  ensembl transcript: ENST00000532927
  gene symbol: FBXO3
  hgvsc: ENST00000532927.1:c.474-1288G>A
  variant of: http://identifiers.org/hgnc/13582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 668
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.25e1
  variant carriers: 686
genotype depth: GenotypeDepth
  all individuals: 20532
  bin: 2.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 3.75e1
  variant carriers: 326
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 234
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.75e1
  variant carriers: 290
genotype depth: GenotypeDepth
  all individuals: 21507
  bin: 2.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.25e1
  variant carriers: 532
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 4.75e1
  variant carriers: 575
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 4.25e1
  variant carriers: 484
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 593
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 441
hgvs: p.Val221Ile
num of homozygotes: 366
reference allele: C

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4324
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2253
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41248
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1368
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2037
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

Latino
type: Population
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

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

FS
type: SiteQuality
SIO_000300: 1.329e1

DP
type: SiteQuality
SIO_000300: 1.778313e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.664e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.029e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11458
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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-1

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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ReadPosRankSum
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DP
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SIO_000300: 1.778313e6

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.628e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.906e1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

DP
type: SiteQuality
SIO_000300: 1.778242e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.08e-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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.727526618956188e-5
allele num: 11458
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

QD
type: SiteQuality
SIO_000300: 1.171e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.906e1

VQSLOD
type: SiteQuality
SIO_000300: 5.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.71e-1

DP
type: SiteQuality
SIO_000300: 1.778242e6

FS
type: SiteQuality
SIO_000300: 1.628e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.08e-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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

QD
type: SiteQuality
SIO_000300: 1.151e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.722e0

DP
type: SiteQuality
SIO_000300: 1.777663e6

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.37e-2

FS
type: SiteQuality
SIO_000300: 8.33e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-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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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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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502810255177181e-5
allele num: 66542
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.154e0

ClippingRankSum
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InbreedingCoeff
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SIO_000300: 1.52e-2

BaseQRankSum
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ReadPosRankSum
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DP
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 902
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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South Asian
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African
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European (Non-Finnish)
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allele frequency: 6.024822267743102e-5
allele num: 66392
num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

Other
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South Asian
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European (Non-Finnish)
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allele frequency: 1.509023963300537e-5
allele num: 66268
num of homozygotes: 0

East Asian
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African
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allele frequency: 9.648784253184099e-5
allele num: 10364
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Latino
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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MQ
type: SiteQuality
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DP
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
type: Population
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African
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.55550024888004e-5
allele num: 64288
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ReadPosRankSum
type: SiteQuality
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FS
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MQRankSum
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QD
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VQSLOD
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DP
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.883e1

GenotypeQuality
all individuals: 1478
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 748
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4312
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5304
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11192
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.337938902268983e-5
allele num: 15778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9914
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

QD
type: SiteQuality
SIO_000300: 1.773e1

VQSLOD
type: SiteQuality
SIO_000300: -1.217e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

FS
type: SiteQuality
SIO_000300: 3.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e0

MQRankSum
type: SiteQuality
SIO_000300: -5.34e-1

DP
type: SiteQuality
SIO_000300: 1.510483e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 101

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.76114902396445e-5
allele num: 63010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15948
num of homozygotes: 0

African
type: Population
allele count: 88
allele frequency: 9.233997901364113e-3
allele num: 9530
num of homozygotes: 1

Latino
type: Population
allele count: 13
allele frequency: 1.184834123222749e-3
allele num: 10972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7996
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.152073732718894e-3
allele num: 868
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

QD
type: SiteQuality
SIO_000300: 1.599e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.44e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

DP
type: SiteQuality
SIO_000300: 1.692435e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 603
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3624
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544067691927614e-5
allele num: 64764
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.753e0

MQRankSum
type: SiteQuality
SIO_000300: -1.441e0

VQSLOD
type: SiteQuality
SIO_000300: 8.699999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.38e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

DP
type: SiteQuality
SIO_000300: 1.811115e6

QD
type: SiteQuality
SIO_000300: 1.33e1

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3766
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523461304082876e-5
allele num: 65640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.623e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.843895e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.77e-1

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
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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
all individuals: 10963
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.006846556584777e-4
allele num: 9932
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522209029743965e-5
allele num: 65694
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.75e0

DP
type: SiteQuality
SIO_000300: 1.845954e6

QD
type: SiteQuality
SIO_000300: 1.118e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.83e-1

FS
type: SiteQuality
SIO_000300: 1.745e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
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variant carriers: 0

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

GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 1733
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508978421608571e-5
allele num: 66270
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: 11416
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10098
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -4.328e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.38e-1

DP
type: SiteQuality
SIO_000300: 1.864078e6

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e0

FS
type: SiteQuality
SIO_000300: 3.771e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
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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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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10098
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: 11416
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508978421608571e-5
allele num: 66270
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e0

DP
type: SiteQuality
SIO_000300: 1.864078e6

VQSLOD
type: SiteQuality
SIO_000300: -4.328e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.771e0

QD
type: SiteQuality
SIO_000300: 1.505e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
all individuals: 37
bin: 3.25e1
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GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.869299e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.5e0

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.919e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 369
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GenotypeQuality
all individuals: 28
bin: 5.75e1
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GenotypeQuality
all individuals: 10983
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 6688
bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 8614
num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 12
allele frequency: 1.806412765316875e-4
allele num: 66430
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.806e0

MQRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: 2.89e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
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SIO_000300: 1.870316e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.345e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-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
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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
allele num: 8618
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16450
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505072092953252e-5
allele num: 66442
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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FS
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MQRankSum
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QD
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BaseQRankSum
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DP
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ClippingRankSum
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SIO_000300: -6.95e-1

MQ
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ReadPosRankSum
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SIO_000300: 1.59e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0.0e0
allele num: 10226
num of homozygotes: 0

European (Finnish)
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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: 2
allele frequency: 3.008604609182261e-5
allele num: 66476
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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allele count: 0
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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

InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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FS
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SIO_000300: 1.594e0

ClippingRankSum
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SIO_000300: -3.72e-1

BaseQRankSum
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VQSLOD
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QD
type: SiteQuality
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DP
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SIO_000300: 1.872052e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 1.3e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66508
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.522e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 1.872413e6

QD
type: SiteQuality
SIO_000300: 1.101e1

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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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66518
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
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Latino
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allele frequency: 8.710801393728223e-5
allele num: 11480
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -1.967e-1

QD
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 1.1e-3

ReadPosRankSum
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SIO_000300: 7.91e-1

BaseQRankSum
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SIO_000300: 4.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-1

DP
type: SiteQuality
SIO_000300: 1.872181e6

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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variant carriers: 0

African
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allele frequency: 9.777082518576456e-5
allele num: 10228
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 frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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Other
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MQRankSum
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
type: SiteQuality
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66530
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South Asian
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European (Finnish)
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African
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allele num: 10224
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Other
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Latino
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VQSLOD
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InbreedingCoeff
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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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QD
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele num: 10242
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South Asian
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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FS
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DP
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 16

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2001

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 535

European (Finnish)
type: Population
allele count: 6602
allele frequency: 1.0e0
allele num: 6602
num of homozygotes: 3301

European (Non-Finnish)
type: Population
allele count: 66543
allele frequency: 9.991441441441441e-1
allele num: 66600
num of homozygotes: 33243

African
type: Population
allele count: 9277
allele frequency: 9.057801210701035e-1
allele num: 10242
num of homozygotes: 4200

Other
type: Population
allele count: 897
allele frequency: 9.922566371681416e-1
allele num: 904
num of homozygotes: 445

South Asian
type: Population
allele count: 16458
allele frequency: 9.979383943730293e-1
allele num: 16492
num of homozygotes: 8212

East Asian
type: Population
allele count: 8633
allele frequency: 9.998841788278897e-1
allele num: 8634
num of homozygotes: 4316

Latino
type: Population
allele count: 11422
allele frequency: 9.946011842563567e-1
allele num: 11484
num of homozygotes: 5680

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.75e-2

FS
type: SiteQuality
SIO_000300: 1.772e0

QD
type: SiteQuality
SIO_000300: 3.135e1

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e-1

DP
type: SiteQuality
SIO_000300: 2.982734e6

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
all individuals: 350
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2884
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 7
allele frequency: 6.403219904866448e-4
allele num: 10932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8032
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.812e0

FS
type: SiteQuality
SIO_000300: 1.423e0

DP
type: SiteQuality
SIO_000300: 1.557229e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

QD
type: SiteQuality
SIO_000300: 1.282e1

VQSLOD
type: SiteQuality
SIO_000300: 3.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

GenotypeQuality
all individuals: 141
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10932
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62506
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.891312570924221e-4
allele num: 15862
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

FS
type: SiteQuality
SIO_000300: 1.423e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.812e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

QD
type: SiteQuality
SIO_000300: 1.282e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.73e0

DP
type: SiteQuality
SIO_000300: 1.557229e6

GenotypeQuality
all individuals: 1059
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2332
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 176
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variant carriers: 0

GenotypeQuality
all individuals: 4688
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variant carriers: 0

GenotypeQuality
all individuals: 2751
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 325
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variant carriers: 0

GenotypeQuality
all individuals: 461
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variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24099
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.614100784452981e-5
allele num: 61954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7930
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.236e0

VQSLOD
type: SiteQuality
SIO_000300: -2.414e0

FS
type: SiteQuality
SIO_000300: 1.6401e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.79e-1

DP
type: SiteQuality
SIO_000300: 1.459839e6

QD
type: SiteQuality
SIO_000300: 3.66e0

GenotypeQuality
all individuals: 4394
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 655
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variant carriers: 0

GenotypeQuality
all individuals: 2321
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.906456532791052e-4
allele num: 15736
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61724
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.521e1

FS
type: SiteQuality
SIO_000300: 2.0266e1

VQSLOD
type: SiteQuality
SIO_000300: -8.856000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.457489e6

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.042e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.274e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

GenotypeQuality
all individuals: 3342
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
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variant carriers: 0

GenotypeQuality
all individuals: 455
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variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4574
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.620115352213077e-5
allele num: 61724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10774
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.856000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.274e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

DP
type: SiteQuality
SIO_000300: 1.457489e6

FS
type: SiteQuality
SIO_000300: 2.0266e1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.042e1

MQ
type: SiteQuality
SIO_000300: 5.521e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

GenotypeQuality
all individuals: 204
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2321
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1025
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11907
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4574
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10774
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61724
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.262945188178833e-4
allele num: 7918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.042e1

VQSLOD
type: SiteQuality
SIO_000300: -8.856000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.274e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

MQ
type: SiteQuality
SIO_000300: 5.521e1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 1.457489e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 2.0266e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.642791431199895e-5
allele num: 60872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7772
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 35
allele frequency: 2.234137622877569e-3
allele num: 15666
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

QD
type: SiteQuality
SIO_000300: 1.035e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

FS
type: SiteQuality
SIO_000300: 3.229e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.6e0

DP
type: SiteQuality
SIO_000300: 1.371206e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.329338127580237e-5
allele num: 60072
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7702
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9224
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.326048e6

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.140000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.661e0

GenotypeQuality
all individuals: 3056
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 311
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variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9092
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.291822761917065e-4
allele num: 15482
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.92e-1

FS
type: SiteQuality
SIO_000300: 3.854e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.42e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 1.270538e6

QD
type: SiteQuality
SIO_000300: 2.477e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.573e0

GenotypeQuality
all individuals: 6287
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
all individuals: 1025
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GenotypeQuality
all individuals: 3145
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 7.030936118923262e-4
allele num: 9956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.767346505955958e-5
allele num: 56582
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.359e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e-1

DP
type: SiteQuality
SIO_000300: 1.212869e6

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 2.297e0

VQSLOD
type: SiteQuality
SIO_000300: 8.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

QD
type: SiteQuality
SIO_000300: 1.098e1

GenotypeQuality
all individuals: 1870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 7.5e0
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 231
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variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11014
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.406395568425028e-4
allele num: 15886
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.500741e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.03e-1

FS
type: SiteQuality
SIO_000300: 8.521000000000001e0

QD
type: SiteQuality
SIO_000300: 1.32e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.78e-1

GenotypeQuality
all individuals: 3762
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3745
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19372
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1874
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GenotypeQuality
all individuals: 875
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variant carriers: 0

GenotypeQuality
all individuals: 5343
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.662786830728301e-5
allele num: 60140
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9246
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10820
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.263e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e-1

QD
type: SiteQuality
SIO_000300: 3.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

DP
type: SiteQuality
SIO_000300: 1.557071e6

MQ
type: SiteQuality
SIO_000300: 5.915e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 787
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3745
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 1188
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GenotypeQuality
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GenotypeQuality
all individuals: 2027
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GenotypeQuality
all individuals: 7334
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variant carriers: 11

GenotypeQuality
all individuals: 1974
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variant carriers: 1

GenotypeQuality
all individuals: 5343
bin: 6.75e1
variant carriers: 1

South Asian
type: Population
allele count: 2
allele frequency: 1.272426517368622e-4
allele num: 15718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.190810465858328e-4
allele num: 6268
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.848428835489834e-4
allele num: 10820
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 6.278252134605726e-4
allele num: 7964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.829065513801131e-4
allele num: 60140
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.163097555699762e-4
allele num: 9246
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 6.263e0

DP
type: SiteQuality
SIO_000300: 1.557071e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

QD
type: SiteQuality
SIO_000300: 3.91e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

GenotypeQuality
all individuals: 1128
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1485
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GenotypeQuality
all individuals: 6751
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.028171910343409e-4
allele num: 9726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63526
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.165e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.666272e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

QD
type: SiteQuality
SIO_000300: 3.117e1

GenotypeQuality
all individuals: 301
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.569957297161517e-5
allele num: 63696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16094
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11230
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.672239e6

FS
type: SiteQuality
SIO_000300: 1.1516e1

QD
type: SiteQuality
SIO_000300: 9.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.848e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567889620570712e-5
allele num: 63780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16100
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.455e0

VQSLOD
type: SiteQuality
SIO_000300: 3.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-1

FS
type: SiteQuality
SIO_000300: 7.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.083e1

DP
type: SiteQuality
SIO_000300: 1.679489e6

GenotypeQuality
all individuals: 7654
bin: 9.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1551
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63966
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.890469416785207e-5
allele num: 11248
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16112
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.032e1

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.684946e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 694
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3361
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 27
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GenotypeQuality
all individuals: 216
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GenotypeQuality
all individuals: 7657
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GenotypeQuality
all individuals: 260
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GenotypeQuality
all individuals: 28880
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GenotypeQuality
all individuals: 2677
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16136
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558360604643914e-5
allele num: 64170
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9818
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.311e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 3.117e0

QD
type: SiteQuality
SIO_000300: 1.712e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.690138e6

GenotypeQuality
all individuals: 285
bin: 2.75e1
variant carriers: 50

GenotypeQuality
all individuals: 13883
bin: 6.25e1
variant carriers: 281

GenotypeQuality
all individuals: 384
bin: 3.25e1
variant carriers: 72

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 31

GenotypeQuality
all individuals: 387
bin: 5.25e1
variant carriers: 215

GenotypeQuality
all individuals: 218
bin: 4.25e1
variant carriers: 87

GenotypeQuality
all individuals: 35481
bin: 9.75e1
variant carriers: 33605

GenotypeQuality
all individuals: 679
bin: 2.25e1
variant carriers: 46

GenotypeQuality
all individuals: 812
bin: 9.25e1
variant carriers: 482

GenotypeQuality
all individuals: 1368
bin: 7.75e1
variant carriers: 435

East Asian
type: Population
allele count: 2506
allele frequency: 2.948929159802307e-1
allele num: 8498
num of homozygotes: 349

African
type: Population
allele count: 3000
allele frequency: 2.972651605231867e-1
allele num: 10092
num of homozygotes: 447

European (Finnish)
type: Population
allele count: 2272
allele frequency: 3.478260869565217e-1
allele num: 6532
num of homozygotes: 383

Other
type: Population
allele count: 349
allele frequency: 3.895089285714285e-1
allele num: 896
num of homozygotes: 62

Latino
type: Population
allele count: 3721
allele frequency: 3.265180765180765e-1
allele num: 11396
num of homozygotes: 624

South Asian
type: Population
allele count: 6133
allele frequency: 3.751070336391437e-1
allele num: 16350
num of homozygotes: 1165

European (Non-Finnish)
type: Population
allele count: 27759
allele frequency: 4.228589708436157e-1
allele num: 65646
num of homozygotes: 5805

QD
type: SiteQuality
SIO_000300: 2.003e1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

FS
type: SiteQuality
SIO_000300: 7.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

DP
type: SiteQuality
SIO_000300: 2.338886e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 787
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2667
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3186
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31341
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515243348081702e-5
allele num: 65996
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.646e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.979149e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.207e0

MQRankSum
type: SiteQuality
SIO_000300: 9.86e-1

QD
type: SiteQuality
SIO_000300: 1.761e1

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2652
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 665
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 620
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variant carriers: 0

GenotypeQuality
all individuals: 374
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variant carriers: 0

GenotypeQuality
all individuals: 31856
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6435
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.567731194187983e-5
allele num: 66070
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.69e-1

QD
type: SiteQuality
SIO_000300: 1.614e1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-1

DP
type: SiteQuality
SIO_000300: 1.981454e6

GenotypeQuality
all individuals: 591
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32950
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9340
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
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variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 3133
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1016
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2623
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variant carriers: 0

GenotypeQuality
all individuals: 6427
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510163399679845e-5
allele num: 66218
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.904e1

DP
type: SiteQuality
SIO_000300: 1.987858e6

VQSLOD
type: SiteQuality
SIO_000300: -1.965e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.056e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.114e0

QD
type: SiteQuality
SIO_000300: 1.342e1

FS
type: SiteQuality
SIO_000300: 1.091e0

GenotypeQuality
all individuals: 33677
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 9338
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1901
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2607
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 136
allele frequency: 1.328125e-2
allele num: 10240
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

Latino
type: Population
allele count: 16
allele frequency: 1.394457033292662e-3
allele num: 11474
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016955288722621e-5
allele num: 66292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.15e0

QD
type: SiteQuality
SIO_000300: 1.227e1

DP
type: SiteQuality
SIO_000300: 1.994876e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.165e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.74e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

GenotypeQuality
all individuals: 167
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 6349
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variant carriers: 1

GenotypeQuality
all individuals: 181
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variant carriers: 0

GenotypeQuality
all individuals: 1907
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variant carriers: 0

GenotypeQuality
all individuals: 439
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 2616
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variant carriers: 0

GenotypeQuality
all individuals: 3133
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66360
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.090875867949811e-5
allele num: 16418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.995845e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.001e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: -7.16e-2

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

GenotypeQuality
all individuals: 437
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
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GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 128
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variant carriers: 0

GenotypeQuality
all individuals: 1911
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variant carriers: 0

GenotypeQuality
all individuals: 1013
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GenotypeQuality
all individuals: 34286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 3133
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.218026796589525e-4
allele num: 16420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
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: 2
allele frequency: 3.013772942346524e-5
allele num: 66362
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQRankSum
type: SiteQuality
SIO_000300: 2.18e0

DP
type: SiteQuality
SIO_000300: 1.996351e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e-1

QD
type: SiteQuality
SIO_000300: 1.049e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.399999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.723000000000001e-1

GenotypeQuality
all individuals: 485
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 2.75e1
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GenotypeQuality
all individuals: 6339
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1009
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GenotypeQuality
all individuals: 3101
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1895
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
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variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.088650754992694e-5
allele num: 16424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66378
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.999906e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

FS
type: SiteQuality
SIO_000300: 1.087e0

QD
type: SiteQuality
SIO_000300: 1.031e1

GenotypeQuality
all individuals: 1006
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 736
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GenotypeQuality
all individuals: 2603
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3100
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.090875867949811e-5
allele num: 16418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.382e0

DP
type: SiteQuality
SIO_000300: 1.998944e6

FS
type: SiteQuality
SIO_000300: 2.611e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 8.17e0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
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: 4
allele frequency: 6.03554938588285e-5
allele num: 66274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.056e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

FS
type: SiteQuality
SIO_000300: 2.507e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 1.992035e6

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 347
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66230
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.299e0

QD
type: SiteQuality
SIO_000300: 9.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e0

DP
type: SiteQuality
SIO_000300: 1.989471e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.996e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 987
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515610791148833e-5
allele num: 65980
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

DP
type: SiteQuality
SIO_000300: 1.955324e6

QD
type: SiteQuality
SIO_000300: 1.008e1

MQRankSum
type: SiteQuality
SIO_000300: -1.559e0

MQ
type: SiteQuality
SIO_000300: 5.766e1

FS
type: SiteQuality
SIO_000300: 3.988e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.07e0

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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516944267467613e-5
allele num: 65922
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.936223e6

FS
type: SiteQuality
SIO_000300: 4.423e0

VQSLOD
type: SiteQuality
SIO_000300: -1.827e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: -4.64e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 4.94e0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16294
num of homozygotes: 0

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

Latino
type: Population
allele count: 4
allele frequency: 3.500175008750437e-4
allele num: 11428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.929216e6

QD
type: SiteQuality
SIO_000300: 1.08e1

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.972e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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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variant carriers: 33

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: 16294
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.917152858809801e-4
allele num: 10284
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.750087504375219e-4
allele num: 11428
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 4.096743847297667e-4
allele num: 65906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.972e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

QD
type: SiteQuality
SIO_000300: 1.08e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

DP
type: SiteQuality
SIO_000300: 1.929216e6

GenotypeQuality
all individuals: 972
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.045159718627242e-5
allele num: 65678
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.762e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.312e0

DP
type: SiteQuality
SIO_000300: 1.861085e6

QD
type: SiteQuality
SIO_000300: 7.13e0

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

VQSLOD
type: SiteQuality
SIO_000300: -8.559e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-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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bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 16
allele frequency: 1.866542230517966e-3
allele num: 8572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65802
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

DP
type: SiteQuality
SIO_000300: 1.576059e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 33225
bin: 6.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517266492686776e-5
allele num: 65908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.054e1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.333e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -6.917e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.605499e6

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.936e1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6695
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 810
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GenotypeQuality
all individuals: 640
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65910
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.100536847242558e-5
allele num: 16392
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.61213e6

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.33e-1

QD
type: SiteQuality
SIO_000300: 1.365e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

East Asian
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allele frequency: 1.163061177017911e-4
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66078
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.043e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.399e0

QD
type: SiteQuality
SIO_000300: 3.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.9e-1

FS
type: SiteQuality
SIO_000300: 1.2357e1

DP
type: SiteQuality
SIO_000300: 1.641238e6

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.079766536964981e-5
allele num: 16448
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.54008898574412e-5
allele num: 66078
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 1.528e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

QD
type: SiteQuality
SIO_000300: 1.212e1

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.744e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

DP
type: SiteQuality
SIO_000300: 1.644813e6

GenotypeQuality
all individuals: 39981
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7025
bin: 6.75e1
variant carriers: 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: 11462
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507204437209863e-5
allele num: 66348
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

FS
type: SiteQuality
SIO_000300: 1.0672e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.963e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.261e0

QD
type: SiteQuality
SIO_000300: 2.14e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 1.663392e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 33
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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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variant carriers: 0

GenotypeQuality
all individuals: 1810
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GenotypeQuality
all individuals: 40007
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506614035616356e-5
allele num: 66374
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.664933e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 1.663e1

FS
type: SiteQuality
SIO_000300: 1.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.032e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66444
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.17e1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.535e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

MQ
type: SiteQuality
SIO_000300: 5.895e1

DP
type: SiteQuality
SIO_000300: 1.668524e6

GenotypeQuality
all individuals: 7040
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 162

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 (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 1.743375174337517e-3
allele num: 11472
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.857280617164899e-4
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 128
allele frequency: 1.925912551533207e-3
allele num: 66462
num of homozygotes: 0

East Asian
type: Population
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: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.065016982047549e-4
allele num: 16488
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

FS
type: SiteQuality
SIO_000300: 6.96e-1

QD
type: SiteQuality
SIO_000300: 1.374e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

DP
type: SiteQuality
SIO_000300: 1.673606e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6556
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.504619180885318e-5
allele num: 66462
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.673606e6

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3