2-26477140-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477140
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477140
    reference: chr 2
allele count: 1
allele frequency: 8.255729476256522e-6
allele num: 121128
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.18C>T
  hgvsp: ENST00000317799.5:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.18C>T
  hgvsp: ENST00000537713.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.97C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.18C>T
  hgvsp: ENST00000405867.3:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.18C>T
  hgvsp: ENST00000412805.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.18C>T
  hgvsp: ENST00000448743.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-132C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.18C>T
  hgvsp: ENST00000425035.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8108
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1911
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr6Tyr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS

2-26477155-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477155
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477154
    reference: chr 2
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.36delC
  hgvsp: ENSP00000385411.3:p.Thr13LeufsTer11
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.36delC
  hgvsp: ENSP00000444295.1:p.Thr13LeufsTer11
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.36delC
  hgvsp: ENSP00000325136.5:p.Thr13LeufsTer11
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.115delC
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.36delC
  hgvsp: ENSP00000413103.1:p.Thr13LeufsTer11
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.36delC
  hgvsp: ENSP00000415300.1:p.Thr13LeufsTer11
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.36delC
  hgvsp: ENSP00000404633.1:p.Thr13LeufsTer11
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-114delC
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 6859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4425
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr13LeufsTer11
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: TC
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/2-26477169-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477169
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477169
    reference: chr 2
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.126A>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-103A>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.47A>C
  hgvsp: ENSP00000325136.5:p.Lys16Thr
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.47A>C
  hgvsp: ENSP00000415300.1:p.Lys16Thr
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.47A>C
  hgvsp: ENSP00000404633.1:p.Lys16Thr
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.47A>C
  hgvsp: ENSP00000444295.1:p.Lys16Thr
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.47A>C
  hgvsp: ENSP00000413103.1:p.Lys16Thr
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.47A>C
  hgvsp: ENSP00000385411.3:p.Lys16Thr
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7078
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys16Thr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

2-26477176-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477176
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477176
    reference: chr 2
allele count: 1
allele frequency: 8.265282507356101e-6
allele num: 120988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.54C>T
  hgvsp: ENST00000405867.3:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.54C>T
  hgvsp: ENST00000425035.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.54C>T
  hgvsp: ENST00000412805.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-96C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.54C>T
  hgvsp: ENST00000448743.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.54C>T
  hgvsp: ENST00000537713.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.133C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.54C>T
  hgvsp: ENST00000317799.5:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala18Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

2-26477183-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477183
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477183
    reference: chr 2
allele count: 1
allele frequency: 8.27787159365584e-6
allele num: 120804
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.61T>G
  hgvsp: ENSP00000325136.5:p.Phe21Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.61T>G
  hgvsp: ENSP00000415300.1:p.Phe21Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.61T>G
  hgvsp: ENSP00000413103.1:p.Phe21Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.61T>G
  hgvsp: ENSP00000385411.3:p.Phe21Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.61T>G
  hgvsp: ENSP00000404633.1:p.Phe21Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.140T>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.61T>G
  hgvsp: ENSP00000444295.1:p.Phe21Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-89T>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6530
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2504
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2710
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe21Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

2-26477186-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477186
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477186
    reference: chr 2
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.64T>C
  hgvsp: ENSP00000413103.1:p.Ser22Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.64T>C
  hgvsp: ENSP00000325136.5:p.Ser22Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.64T>C
  hgvsp: ENSP00000404633.1:p.Ser22Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.64T>C
  hgvsp: ENSP00000444295.1:p.Ser22Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.64T>C
  hgvsp: ENSP00000385411.3:p.Ser22Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.64T>C
  hgvsp: ENSP00000415300.1:p.Ser22Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.143T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-86T>C
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2702
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2531
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser22Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

2-26477189-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477189
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477189
    reference: chr 2
allele count: 2
allele frequency: 1.657412778652524e-5
allele num: 120670
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.64+3A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.64+3A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.64+3A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.64+3A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.64+3A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.143+3A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-86+3A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.64+3A>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3872
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2529
  bin: 8.25e1
  variant carriers: 0
hgvs: c.64+3A>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

2-26477196-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477196
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477196
    reference: chr 2
allele count: 1
allele frequency: 8.313519445321983e-6
allele num: 120286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.64+10T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-86+10T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.143+10T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.64+10T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.64+10T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.64+10T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.64+10T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.64+10T>C
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37588
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

2-26477197-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477197
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477197
    reference: chr 2
allele count: 48
allele frequency: 3.990356638124533e-4
allele num: 120290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.64+11T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.64+11T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.64+11T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.64+11T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.143+11T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.64+11T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.64+11T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-86+11T>C
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5760
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8105
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3102
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

2-26477200-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477200
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477199
    reference: chr 2
allele count: 32
allele frequency: 2.674511901577962e-4
allele num: 119648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.64+15delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.64+15delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.64+15delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.64+15delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.64+15delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.143+15delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-86+15delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.64+15delA
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5434
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3419
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: TA
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

2-26477201-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477201
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477201
    reference: chr 2
allele count: 1
allele frequency: 8.35812911637859e-6
allele num: 119644
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.143+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.64+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.64+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.64+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.64+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.64+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-86+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.64+15A>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5743
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8082
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

2-26477201-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477201
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477200
    reference: chr 2
allele count: 1
allele frequency: 8.35812911637859e-6
allele num: 119644
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.64+22delT
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.143+22delT
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.64+22delT
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.64+22delT
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.64+22delT
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.64+22delT
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.64+22delT
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-86+22delT
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8082
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5743
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2443
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3651
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1013
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: AT
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD

2-26477207-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477207
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477207
    reference: chr 2
allele count: 1
allele frequency: 8.347106058329577e-6
allele num: 119802
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.64+21T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.143+21T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-86+21T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.64+21T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.64+21T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.64+21T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.64+21T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.64+21T>A
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8090
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4408
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2116
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

2-26477234-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477234
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477234
    reference: chr 2
allele count: 2
allele frequency: 1.660357308892874e-5
allele num: 120456
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.64+48A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.64+48A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.64+48A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-86+48A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.143+48A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.64+48A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.64+48A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.64+48A>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5010
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8090
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5638
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2317
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/2-26477247-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477247
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477247
    reference: chr 2
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.65-51A>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.65-51A>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.144-51A>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.65-51A>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.65-51A>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.65-51A>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-85-51A>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.65-51A>C
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22251
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28595
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

2-26477265-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477265
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477265
    reference: chr 2
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.65-33T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-85-33T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.65-33T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.65-33T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.65-33T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.65-33T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.144-33T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.65-33T>C
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2634
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1067
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

2-26477267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477267
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477267
    reference: chr 2
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.65-31C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.65-31C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-85-31C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.144-31C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.65-31C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.65-31C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.65-31C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.65-31C>T
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1646
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7736
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29739
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
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: C
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

2-26477268-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477268
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477268
    reference: chr 2
allele count: 2
allele frequency: 1.649647800194658e-5
allele num: 121238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.65-30T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.65-30T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.144-30T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.65-30T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-85-30T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.65-30T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.65-30T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.65-30T>A
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3323
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1647
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

2-26477279-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477279
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477279
    reference: chr 2
allele count: 3
allele frequency: 2.474757473767571e-5
allele num: 121224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.65-19A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.65-19A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.65-19A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-85-19A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.144-19A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.65-19A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.65-19A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.65-19A>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2496
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11387
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1064
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7718
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

2-26477280-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477280
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477280
    reference: chr 2
allele count: 5
allele frequency: 4.125752949913359e-5
allele num: 121190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.65-18G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-85-18G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.65-18G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.144-18G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.65-18G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.65-18G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.65-18G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.65-18G>T
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 22434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1644
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11352
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

2-26477283-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477283
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477283
    reference: chr 2
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.65-15T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.144-15T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.65-15T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.65-15T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.65-15T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.65-15T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.65-15T>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-85-15T>A
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2625
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7708
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

2-26477284-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477284
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477284
    reference: chr 2
allele count: 11
allele frequency: 9.082652134423252e-5
allele num: 121110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.65-14A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.65-14A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.65-14A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.65-14A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.144-14A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-85-14A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.65-14A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.65-14A>T
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22430
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29828
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7693
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

2-26477290-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477290
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477290
    reference: chr 2
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.65-8T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.65-8T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.65-8T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.65-8T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-85-8T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.144-8T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.65-8T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.65-8T>C
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29742
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.25e1
  variant carriers: 0
hgvs: c.65-8T>C
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

2-26477293-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477293
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477293
    reference: chr 2
allele count: 272
allele frequency: 2.309115914223135e-3
allele num: 117794
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.65-5T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.65-5T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-85-5T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.144-5T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.65-5T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.65-5T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.65-5T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.65-5T>C
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 4.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 22410
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 13487
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 3.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 2532
  bin: 7.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 3.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 8.75e1
  variant carriers: 9
hgvs: c.65-5T>C
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-26477300-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477300
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477300
    reference: chr 2
allele count: 7
allele frequency: 5.776721462995973e-5
allele num: 121176
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.67A>G
  hgvsp: ENSP00000325136.5:p.Ile23Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.67A>G
  hgvsp: ENSP00000444295.1:p.Ile23Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.67A>G
  hgvsp: ENSP00000404633.1:p.Ile23Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.146A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.67A>G
  hgvsp: ENSP00000413103.1:p.Ile23Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.67A>G
  hgvsp: ENSP00000385411.3:p.Ile23Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.67A>G
  hgvsp: ENSP00000415300.1:p.Ile23Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-83A>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile23Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

2-26477302-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477302
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477302
    reference: chr 2
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.69A>G
  hgvsp: ENSP00000415300.1:p.Ile23Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.69A>G
  hgvsp: ENSP00000413103.1:p.Ile23Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.69A>G
  hgvsp: ENSP00000404633.1:p.Ile23Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.69A>G
  hgvsp: ENSP00000385411.3:p.Ile23Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-81A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.148A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.69A>G
  hgvsp: ENSP00000444295.1:p.Ile23Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.69A>G
  hgvsp: ENSP00000325136.5:p.Ile23Met
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2420
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile23Met
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP

2-26477320-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477320
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477320
    reference: chr 2
allele count: 2
allele frequency: 1.652237129072764e-5
allele num: 121048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.87C>T
  hgvsp: ENST00000405867.3:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.87C>T
  hgvsp: ENST00000412805.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.87C>T
  hgvsp: ENST00000448743.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-63C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.87C>T
  hgvsp: ENST00000537713.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.87C>T
  hgvsp: ENST00000425035.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.87C>T
  hgvsp: ENST00000317799.5:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.166C>T
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2415
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser29Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-26477323-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477323
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477323
    reference: chr 2
allele count: 3
allele frequency: 2.478929102627665e-5
allele num: 121020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-60C>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.90C>G
  hgvsp: ENST00000537713.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.90C>G
  hgvsp: ENST00000317799.5:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.90C>G
  hgvsp: ENST00000448743.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.90C>G
  hgvsp: ENST00000425035.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.90C>G
  hgvsp: ENST00000405867.3:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.169C>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.90C>G
  hgvsp: ENST00000412805.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7823
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3266
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2593
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser30Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

2-26477324-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477324
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477324
    reference: chr 2
allele count: 2
allele frequency: 1.653083827880912e-5
allele num: 120986
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-59C>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.91C>G
  hgvsp: ENSP00000325136.5:p.Gln31Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.91C>G
  hgvsp: ENSP00000444295.1:p.Gln31Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.91C>G
  hgvsp: ENSP00000385411.3:p.Gln31Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.91C>G
  hgvsp: ENSP00000404633.1:p.Gln31Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.91C>G
  hgvsp: ENSP00000415300.1:p.Gln31Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.91C>G
  hgvsp: ENSP00000413103.1:p.Gln31Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.170C>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10567
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2415
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln31Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

2-26477324-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477324
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477324
    reference: chr 2
allele count: 1
allele frequency: 8.26541913940456e-6
allele num: 120986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.91C>T
  hgvsp: ENSP00000415300.1:p.Gln31Ter
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.91C>T
  hgvsp: ENSP00000413103.1:p.Gln31Ter
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.91C>T
  hgvsp: ENSP00000385411.3:p.Gln31Ter
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.170C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.91C>T
  hgvsp: ENSP00000444295.1:p.Gln31Ter
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.91C>T
  hgvsp: ENSP00000404633.1:p.Gln31Ter
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-59C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.91C>T
  hgvsp: ENSP00000325136.5:p.Gln31Ter
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2593
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln31Ter
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-26477327-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477327
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477327
    reference: chr 2
allele count: 1
allele frequency: 8.267469162340024e-6
allele num: 120956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.94C>G
  hgvsp: ENSP00000415300.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.94C>G
  hgvsp: ENSP00000404633.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-56C>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.94C>G
  hgvsp: ENSP00000385411.3:p.Leu32Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.94C>G
  hgvsp: ENSP00000444295.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.94C>G
  hgvsp: ENSP00000413103.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.94C>G
  hgvsp: ENSP00000325136.5:p.Leu32Val
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.173C>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu32Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

2-26477328-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477328
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477328
    reference: chr 2
allele count: 1
allele frequency: 8.267469162340024e-6
allele num: 120956
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.95T>C
  hgvsp: ENSP00000415300.1:p.Leu32Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-55T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.95T>C
  hgvsp: ENSP00000404633.1:p.Leu32Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.95T>C
  hgvsp: ENSP00000413103.1:p.Leu32Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.174T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.95T>C
  hgvsp: ENSP00000444295.1:p.Leu32Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.95T>C
  hgvsp: ENSP00000385411.3:p.Leu32Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.95T>C
  hgvsp: ENSP00000325136.5:p.Leu32Pro
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3261
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7817
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu32Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

2-26477330-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477330
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477330
    reference: chr 2
allele count: 1
allele frequency: 8.273899157717065e-6
allele num: 120862
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.97C>T
  hgvsp: ENSP00000444295.1:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.97C>T
  hgvsp: ENSP00000415300.1:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-53C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.176C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.97C>T
  hgvsp: ENSP00000404633.1:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.97C>T
  hgvsp: ENSP00000325136.5:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.97C>T
  hgvsp: ENSP00000385411.3:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.97C>T
  hgvsp: ENSP00000413103.1:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30699
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3253
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7793
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg33Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

2-26477331-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477331
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477331
    reference: chr 2
allele count: 2
allele frequency: 1.654807214959457e-5
allele num: 120860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.98G>A
  hgvsp: ENSP00000444295.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.98G>A
  hgvsp: ENSP00000404633.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.98G>A
  hgvsp: ENSP00000413103.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.98G>A
  hgvsp: ENSP00000415300.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.177G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-52G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.98G>A
  hgvsp: ENSP00000385411.3:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.98G>A
  hgvsp: ENSP00000325136.5:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7789
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg33Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

2-26477339-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477339
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477339
    reference: chr 2
allele count: 3
allele frequency: 2.488346245085516e-5
allele num: 120562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.106C>T
  hgvsp: ENSP00000385411.3:p.Pro36Ser
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.106C>T
  hgvsp: ENSP00000325136.5:p.Pro36Ser
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.106C>T
  hgvsp: ENSP00000413103.1:p.Pro36Ser
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.106C>T
  hgvsp: ENSP00000404633.1:p.Pro36Ser
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.185C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.106C>T
  hgvsp: ENSP00000415300.1:p.Pro36Ser
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.106C>T
  hgvsp: ENSP00000444295.1:p.Pro36Ser
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1603
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro36Ser
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

2-26477342-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477342
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477342
    reference: chr 2
allele count: 4
allele frequency: 3.322645490339408e-5
allele num: 120386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.109G>C
  hgvsp: ENSP00000404633.1:p.Ala37Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.109G>C
  hgvsp: ENSP00000385411.3:p.Ala37Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.109G>C
  hgvsp: ENSP00000415300.1:p.Ala37Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.188G>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.109G>C
  hgvsp: ENSP00000444295.1:p.Ala37Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.109G>C
  hgvsp: ENSP00000413103.1:p.Ala37Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-41G>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.109G>C
  hgvsp: ENSP00000325136.5:p.Ala37Pro
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7707
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala37Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

2-26477346-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477346
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477346
    reference: chr 2
allele count: 1
allele frequency: 8.335556148306214e-6
allele num: 119968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.192C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.109+4C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-41+4C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.109+4C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.109+4C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.109+4C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.109+4C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.109+4C>T
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1339
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1600
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 8.75e1
  variant carriers: 0
hgvs: c.109+4C>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-26477347-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477347
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477347
    reference: chr 2
allele count: 10
allele frequency: 8.34599142032082e-5
allele num: 119818
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.193A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-41+5A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.109+5A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.109+5A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.109+5A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.109+5A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.109+5A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.109+5A>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13530
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10549
  bin: 9.75e1
  variant carriers: 10
hgvs: c.109+5A>G
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

2-26477366-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26477366
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26477366
    reference: chr 2
allele count: 1
allele frequency: 8.454800635801008e-6
allele num: 118276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.109+24A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.109+24A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000479347
  gene symbol: HADHB
  hgvsc: ENST00000479347.1:n.212A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.-41+24A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.109+24A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.109+24A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.109+24A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.109+24A>T
  variant of: http://identifiers.org/hgnc/4803
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11615
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23963
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2363
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

2-26483897-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26483897
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26483897
    reference: chr 2
allele count: 12
allele frequency: 1.11794298490777e-3
allele num: 10734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.492G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.110-2351G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.110-2351G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.110-2351G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.110-2351G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.9G>T
  hgvsp: ENST00000545822.1:c.9G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.110-2351G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.110-2351G>T
  variant of: http://identifiers.org/hgnc/4803
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1807
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu3Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

2-26483909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26483909
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26483909
    reference: chr 2
allele count: 2
allele frequency: 1.862891207153502e-4
allele num: 10736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.110-2339G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.110-2339G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.110-2339G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.110-2339G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.21G>A
  hgvsp: ENSP00000442665.1:p.Trp7Ter
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.110-2339G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.504G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.110-2339G>A
  variant of: http://identifiers.org/hgnc/4803
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3299
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Trp7Ter
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD

2-26483914-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26483914
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26483914
    reference: chr 2
allele count: 2
allele frequency: 1.862544235425591e-4
allele num: 10738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.110-2334T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.509T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.110-2334T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.26T>C
  hgvsp: ENSP00000442665.1:p.Leu9Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.110-2334T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.110-2334T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.110-2334T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.110-2334T>C
  variant of: http://identifiers.org/hgnc/4803
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu9Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

2-26483924-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26483924
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26483924
    reference: chr 2
allele count: 1
allele frequency: 9.324878776575905e-5
allele num: 10724
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.110-2324G>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.36G>C
  hgvsp: ENSP00000442665.1:p.Trp12Cys
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.110-2324G>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.519G>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.110-2324G>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.110-2324G>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.110-2324G>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.110-2324G>C
  variant of: http://identifiers.org/hgnc/4803
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1609
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Trp12Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

2-26486205-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486205
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486205
    reference: chr 2
allele count: 21
allele frequency: 2.109831816263789e-4
allele num: 99534
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.110-43A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.44-43A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.110-43A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.110-43A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.110-43A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.110-43A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1057-43A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.110-43A>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6641
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17777
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3311
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6881
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1964
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

2-26486209-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486209
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486209
    reference: chr 2
allele count: 4
allele frequency: 3.96000396000396e-5
allele num: 101010
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.110-39T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1057-39T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.110-39T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.44-39T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.110-39T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.110-39T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.110-39T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.110-39T>C
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21885
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9253
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7632
  bin: 2.25e1
  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: T
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

2-26486213-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486213
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486213
    reference: chr 2
allele count: 4
allele frequency: 3.867649049525246e-5
allele num: 103422
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1057-35A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.44-35A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.110-35A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.110-35A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.110-35A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.110-35A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.110-35A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.110-35A>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22817
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9270
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-26486221-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486221
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486221
    reference: chr 2
allele count: 7
allele frequency: 6.219236988467758e-5
allele num: 112554
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.110-27T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.44-27T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1057-27T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.110-27T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.110-27T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.110-27T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.110-27T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.110-27T>C
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9521
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7347
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP

2-26486250-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486250
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486250
    reference: chr 2
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.112G>T
  hgvsp: ENSP00000325136.5:p.Val38Phe
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.112G>T
  hgvsp: ENSP00000444295.1:p.Val38Phe
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.46G>T
  hgvsp: ENSP00000442665.1:p.Val16Phe
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.112G>T
  hgvsp: ENSP00000415300.1:p.Val38Phe
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1059G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.112G>T
  hgvsp: ENSP00000385411.3:p.Val38Phe
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.112G>T
  hgvsp: ENSP00000413103.1:p.Val38Phe
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.112G>T
  hgvsp: ENSP00000404633.1:p.Val38Phe
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val38Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

2-26486254-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486254
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486254
    reference: chr 2
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.116A>G
  hgvsp: ENSP00000444295.1:p.Gln39Arg
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.116A>G
  hgvsp: ENSP00000413103.1:p.Gln39Arg
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.116A>G
  hgvsp: ENSP00000415300.1:p.Gln39Arg
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.116A>G
  hgvsp: ENSP00000404633.1:p.Gln39Arg
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.116A>G
  hgvsp: ENSP00000385411.3:p.Gln39Arg
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.116A>G
  hgvsp: ENSP00000325136.5:p.Gln39Arg
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1063A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.50A>G
  hgvsp: ENSP00000442665.1:p.Gln17Arg
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2787
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln39Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

2-26486263-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486263
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486263
    reference: chr 2
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.125C>T
  hgvsp: ENSP00000325136.5:p.Thr42Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.125C>T
  hgvsp: ENSP00000415300.1:p.Thr42Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.125C>T
  hgvsp: ENSP00000444295.1:p.Thr42Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1072C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.125C>T
  hgvsp: ENSP00000404633.1:p.Thr42Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.125C>T
  hgvsp: ENSP00000385411.3:p.Thr42Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.59C>T
  hgvsp: ENSP00000442665.1:p.Thr20Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.125C>T
  hgvsp: ENSP00000413103.1:p.Thr42Met
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7751
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9314
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr42Met
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

2-26486272-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486272
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486272
    reference: chr 2
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.134C>T
  hgvsp: ENSP00000415300.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.134C>T
  hgvsp: ENSP00000413103.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.134C>T
  hgvsp: ENSP00000325136.5:p.Thr45Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.68C>T
  hgvsp: ENSP00000442665.1:p.Thr23Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.134C>T
  hgvsp: ENSP00000404633.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.134C>T
  hgvsp: ENSP00000385411.3:p.Thr45Met
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1081C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.134C>T
  hgvsp: ENSP00000444295.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9314
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr45Met
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

2-26486273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486273
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486273
    reference: chr 2
allele count: 118
allele frequency: 9.719613851273435e-4
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.69G>A
  hgvsp: ENST00000545822.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1082G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.135G>A
  hgvsp: ENST00000425035.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.135G>A
  hgvsp: ENST00000537713.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.135G>A
  hgvsp: ENST00000317799.5:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.135G>A
  hgvsp: ENST00000405867.3:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.135G>A
  hgvsp: ENST00000412805.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.135G>A
  hgvsp: ENST00000448743.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 34618
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9384
  bin: 9.75e1
  variant carriers: 115
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr45Thr
num of homozygotes: 3
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

2-26486273-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486273
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486273
    reference: chr 2
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.69G>T
  hgvsp: ENST00000545822.1:c.69G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.135G>T
  hgvsp: ENST00000412805.1:c.135G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.135G>T
  hgvsp: ENST00000425035.1:c.135G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.135G>T
  hgvsp: ENST00000317799.5:c.135G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.135G>T
  hgvsp: ENST00000448743.1:c.135G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.135G>T
  hgvsp: ENST00000405867.3:c.135G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1082G>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.135G>T
  hgvsp: ENST00000537713.1:c.135G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2779
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr45Thr
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS

2-26486292-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486292
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486292
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.154A>T
  hgvsp: ENSP00000413103.1:p.Arg52Trp
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.154A>T
  hgvsp: ENSP00000385411.3:p.Arg52Trp
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.154A>T
  hgvsp: ENSP00000444295.1:p.Arg52Trp
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.154A>T
  hgvsp: ENSP00000325136.5:p.Arg52Trp
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.154A>T
  hgvsp: ENSP00000415300.1:p.Arg52Trp
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1101A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.88A>T
  hgvsp: ENSP00000442665.1:p.Arg30Trp
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.154A>T
  hgvsp: ENSP00000404633.1:p.Arg52Trp
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34659
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2785
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg52Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD

2-26486309-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486309
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486309
    reference: chr 2
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.171G>A
  hgvsp: ENST00000448743.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.171G>A
  hgvsp: ENST00000425035.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1118G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.105G>A
  hgvsp: ENST00000545822.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.171G>A
  hgvsp: ENST00000537713.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.171G>A
  hgvsp: ENST00000405867.3:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.171G>A
  hgvsp: ENST00000317799.5:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.171G>A
  hgvsp: ENST00000412805.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val57Val
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

2-26486311-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486311
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486311
    reference: chr 2
allele count: 5
allele frequency: 4.11834475487612e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.173A>G
  hgvsp: ENSP00000444295.1:p.Asp58Gly
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.173A>G
  hgvsp: ENSP00000413103.1:p.Asp58Gly
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1120A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.173A>G
  hgvsp: ENSP00000404633.1:p.Asp58Gly
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.173A>G
  hgvsp: ENSP00000415300.1:p.Asp58Gly
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.107A>G
  hgvsp: ENSP00000442665.1:p.Asp36Gly
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.173A>G
  hgvsp: ENSP00000325136.5:p.Asp58Gly
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.173A>G
  hgvsp: ENSP00000385411.3:p.Asp58Gly
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp58Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

2-26486312-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486312
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486312
    reference: chr 2
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.174T>G
  hgvsp: ENSP00000404633.1:p.Asp58Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.174T>G
  hgvsp: ENSP00000385411.3:p.Asp58Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.108T>G
  hgvsp: ENSP00000442665.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1121T>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.174T>G
  hgvsp: ENSP00000444295.1:p.Asp58Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.174T>G
  hgvsp: ENSP00000325136.5:p.Asp58Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.174T>G
  hgvsp: ENSP00000415300.1:p.Asp58Glu
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.174T>G
  hgvsp: ENSP00000413103.1:p.Asp58Glu
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2785
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp58Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

2-26486319-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486319
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486319
    reference: chr 2
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.115C>T
  hgvsp: ENSP00000442665.1:p.Arg39Cys
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.181C>T
  hgvsp: ENSP00000444295.1:p.Arg61Cys
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.181C>T
  hgvsp: ENSP00000415300.1:p.Arg61Cys
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.181C>T
  hgvsp: ENSP00000325136.5:p.Arg61Cys
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.181C>T
  hgvsp: ENSP00000413103.1:p.Arg61Cys
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.181C>T
  hgvsp: ENSP00000404633.1:p.Arg61Cys
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.181C>T
  hgvsp: ENSP00000385411.3:p.Arg61Cys
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1128C>T
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg61Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

2-26486320-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486320
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486320
    reference: chr 2
allele count: 6
allele frequency: 4.942013705851344e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.116G>A
  hgvsp: ENSP00000442665.1:p.Arg39His
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.182G>A
  hgvsp: ENSP00000444295.1:p.Arg61His
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.182G>A
  hgvsp: ENSP00000415300.1:p.Arg61His
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.182G>A
  hgvsp: ENSP00000385411.3:p.Arg61His
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.182G>A
  hgvsp: ENSP00000404633.1:p.Arg61His
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.182G>A
  hgvsp: ENSP00000325136.5:p.Arg61His
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1129G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.182G>A
  hgvsp: ENSP00000413103.1:p.Arg61His
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34648
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7757
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg61His
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ

2-26486322-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486322
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486322
    reference: chr 2
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.118A>G
  hgvsp: ENSP00000442665.1:p.Thr40Ala
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.184A>G
  hgvsp: ENSP00000413103.1:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.184A>G
  hgvsp: ENSP00000444295.1:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.184A>G
  hgvsp: ENSP00000325136.5:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.184A>G
  hgvsp: ENSP00000385411.3:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.184A>G
  hgvsp: ENSP00000404633.1:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.184A>G
  hgvsp: ENSP00000415300.1:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1131A>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34652
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9321
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr62Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

2-26486337-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486337
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486337
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.133T>C
  hgvsp: ENSP00000442665.1:p.Ser45Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.199T>C
  hgvsp: ENSP00000415300.1:p.Ser67Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.199T>C
  hgvsp: ENSP00000325136.5:p.Ser67Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.199T>C
  hgvsp: ENSP00000404633.1:p.Ser67Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.199T>C
  hgvsp: ENSP00000444295.1:p.Ser67Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1146T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.199T>C
  hgvsp: ENSP00000413103.1:p.Ser67Pro
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.199T>C
  hgvsp: ENSP00000385411.3:p.Ser67Pro
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34649
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser67Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

2-26486342-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486342
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486342
    reference: chr 2
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.138C>T
  hgvsp: ENST00000545822.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.204C>T
  hgvsp: ENST00000425035.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.204C>T
  hgvsp: ENST00000448743.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1151C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.204C>T
  hgvsp: ENST00000412805.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.204C>T
  hgvsp: ENST00000405867.3:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.204C>T
  hgvsp: ENST00000317799.5:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.204C>T
  hgvsp: ENST00000537713.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34634
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2785
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly68Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

2-26486348-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486348
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486348
    reference: chr 2
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.209+1G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.209+1G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1156+1G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.209+1G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.143+1G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.209+1G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.209+1G>A
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.209+1G>A
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: c.209+1G>A
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

2-26486354-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486354
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486354
    reference: chr 2
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.209+7A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.209+7A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.209+7A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1156+7A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.209+7A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.143+7A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.209+7A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.209+7A>T
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2785
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 7.25e1
  variant carriers: 0
hgvs: c.209+7A>T
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum

2-26486362-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486362
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486362
    reference: chr 2
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1156+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.209+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.209+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.209+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.209+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.209+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.143+15A>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.209+15A>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7724
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-26486363-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486363
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486363
    reference: chr 2
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.209+16T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.209+16T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1156+16T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.143+16T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.209+16T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.209+16T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.209+16T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.209+16T>C
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9323
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2783
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2590
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

2-26486369-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486369
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486368
    reference: chr 2
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.209+23delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.209+23delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.209+23delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1156+23delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.209+23delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.143+23delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.209+23delA
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.209+23delA
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33561
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: TA
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP

2-26486370-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486370
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486370
    reference: chr 2
allele count: 4
allele frequency: 3.301528607745386e-5
allele num: 121156
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.209+23A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.209+23A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.209+23A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.209+23A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.143+23A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.209+23A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.209+23A>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1156+23A>T
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9327
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

2-26486379-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486379
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486379
    reference: chr 2
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.143+32C>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.209+32C>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.209+32C>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.209+32C>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1156+32C>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.209+32C>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.209+32C>G
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.209+32C>G
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30509
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

2-26486379-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486379
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486379
    reference: chr 2
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.209+32C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.143+32C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1156+32C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.209+32C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.209+32C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.209+32C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.209+32C>T
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.209+32C>T
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2538
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7395
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD

2-26486381-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 26486381
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 26486381
    reference: chr 2
allele count: 1
allele frequency: 8.263506701703935e-6
allele num: 121014
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000444295
  ensembl transcript: ENST00000537713
  gene symbol: HADHB
  hgvsc: ENST00000537713.1:c.209+34T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000413103
  ensembl transcript: ENST00000412805
  gene symbol: HADHB
  hgvsc: ENST00000412805.1:c.209+34T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000442665
  ensembl transcript: ENST00000545822
  gene symbol: HADHB
  hgvsc: ENST00000545822.1:c.143+34T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000325136
  ensembl transcript: ENST00000317799
  gene symbol: HADHB
  hgvsc: ENST00000317799.5:c.209+34T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000415300
  ensembl transcript: ENST00000448743
  gene symbol: HADHB
  hgvsc: ENST00000448743.1:c.209+34T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000404633
  ensembl transcript: ENST00000425035
  gene symbol: HADHB
  hgvsc: ENST00000425035.1:c.209+34T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl transcript: ENST00000494615
  gene symbol: HADHB
  hgvsc: ENST00000494615.1:n.1156+34T>C
  variant of: http://identifiers.org/hgnc/4803
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138029
  ensembl protein: ENSP00000385411
  ensembl transcript: ENST00000405867
  gene symbol: HADHB
  hgvsc: ENST00000405867.3:c.209+34T>C
  variant of: http://identifiers.org/hgnc/4803
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10279
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 2795
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2514
bin: 9.25e1
variant carriers: 0

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

Other
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European (Finnish)
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allele num: 6614
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Latino
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South Asian
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African
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European (Non-Finnish)
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QD
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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Other
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European (Non-Finnish)
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African
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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DP
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VQSLOD
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QD
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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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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.499745043342632e-5
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MQRankSum
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MQ
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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South Asian
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DP
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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European (Finnish)
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Latino
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African
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South Asian
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Other
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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DP
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FS
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QD
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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East Asian
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South Asian
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African
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European (Non-Finnish)
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Other
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VQSLOD
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MQRankSum
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MQ
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DP
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ClippingRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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East Asian
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South Asian
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Latino
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African
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European (Finnish)
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VQSLOD
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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ReadPosRankSum
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FS
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QD
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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MQ
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SIO_000300: 5.78e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

GenotypeQuality
all individuals: 37574
bin: 9.75e1
variant carriers: 32

GenotypeQuality
all individuals: 228
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2441
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2211
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.025430680885972e-4
allele num: 9752
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 3.951127591027901e-4
allele num: 65804
num of homozygotes: 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: 11568
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.043213633597079e-4
allele num: 16430
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.505185e6

FS
type: SiteQuality
SIO_000300: 2.652e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

MQ
type: SiteQuality
SIO_000300: 5.74e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.25e-2

QD
type: SiteQuality
SIO_000300: 1.397e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.68e-1

GenotypeQuality
all individuals: 1197
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3651
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37545
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1265
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65790
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.899e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.57e-1

DP
type: SiteQuality
SIO_000300: 3.50102e6

MQ
type: SiteQuality
SIO_000300: 5.847e1

FS
type: SiteQuality
SIO_000300: 8.625e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e0

MQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
all individuals: 2210
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37545
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1197
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2238
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variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 636
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 8.75e1
variant carriers: 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: 9756
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.085686465433301e-5
allele num: 16432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65790
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.847e1

DP
type: SiteQuality
SIO_000300: 3.50102e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

MQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

FS
type: SiteQuality
SIO_000300: 8.625e0

QD
type: SiteQuality
SIO_000300: 1.899e1

GenotypeQuality
all individuals: 1402
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2220
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 146
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variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517174414370676e-5
allele num: 65912
num of homozygotes: 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: 11566
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.848e0

FS
type: SiteQuality
SIO_000300: 1.129e0

DP
type: SiteQuality
SIO_000300: 3.495992e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.549e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 1.281e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.72e-1

MQ
type: SiteQuality
SIO_000300: 5.658e1

VQSLOD
type: SiteQuality
SIO_000300: -1.097e0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2600
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variant carriers: 0

GenotypeQuality
all individuals: 7712
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variant carriers: 0

GenotypeQuality
all individuals: 1010
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variant carriers: 0

GenotypeQuality
all individuals: 1438
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variant carriers: 0

GenotypeQuality
all individuals: 143
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variant carriers: 0

GenotypeQuality
all individuals: 37594
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2466
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-5
allele num: 66140
num of homozygotes: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.584e0

MQ
type: SiteQuality
SIO_000300: 5.815e1

MQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.69e-1

FS
type: SiteQuality
SIO_000300: 3.765e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.23e-1

QD
type: SiteQuality
SIO_000300: 1.771e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.47e0

DP
type: SiteQuality
SIO_000300: 3.509186e6

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

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 11412
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1661
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variant carriers: 0

GenotypeQuality
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 7846
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variant carriers: 0

GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 1086
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variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.333e0

DP
type: SiteQuality
SIO_000300: 2.13548e6

FS
type: SiteQuality
SIO_000300: 1.623e0

VQSLOD
type: SiteQuality
SIO_000300: 5.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.546e1

MQRankSum
type: SiteQuality
SIO_000300: -7.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 100
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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: 71
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7761
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variant carriers: 0

GenotypeQuality
all individuals: 3329
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.58e-1

DP
type: SiteQuality
SIO_000300: 2.136151e6

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.62e1

MQ
type: SiteQuality
SIO_000300: 5.812e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.626e0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11391
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variant carriers: 1

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1065
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GenotypeQuality
all individuals: 2626
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GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 3321
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variant carriers: 0

GenotypeQuality
all individuals: 2493
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501817198810561e-5
allele num: 66586
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.136476e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.021e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

QD
type: SiteQuality
SIO_000300: 1.924e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.057e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 50
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2495
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 29836
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GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.925669170036588e-4
allele num: 10386
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66588
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

MQ
type: SiteQuality
SIO_000300: 5.87e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e-1

FS
type: SiteQuality
SIO_000300: 5.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-2

DP
type: SiteQuality
SIO_000300: 2.136644e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.42e-1

QD
type: SiteQuality
SIO_000300: 1.369e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 29883
bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.592016588906169e-4
allele num: 11574
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.141e0

DP
type: SiteQuality
SIO_000300: 2.136587e6

FS
type: SiteQuality
SIO_000300: 2.405e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.206e1

VQSLOD
type: SiteQuality
SIO_000300: 6.14e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.575757575757576e-4
allele num: 6600
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -4.201e1

MQRankSum
type: SiteQuality
SIO_000300: -3.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

FS
type: SiteQuality
SIO_000300: 9.2574e1

QD
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.282e0

ReadPosRankSum
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SIO_000300: -1.311e0

DP
type: SiteQuality
SIO_000300: 2.136551e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

MQ
type: SiteQuality
SIO_000300: 5.791e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502133028901039e-5
allele num: 66572
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

FS
type: SiteQuality
SIO_000300: 2.739e0

VQSLOD
type: SiteQuality
SIO_000300: 3.34e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 1.042e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.44e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

DP
type: SiteQuality
SIO_000300: 2.136442e6

GenotypeQuality
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variant carriers: 1

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

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.591861524445794e-4
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.515632515632516e-5
allele num: 66528
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.33747e2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.116e0

VQSLOD
type: SiteQuality
SIO_000300: -8.556999999999999e1

MQ
type: SiteQuality
SIO_000300: 5.824e1

DP
type: SiteQuality
SIO_000300: 2.136398e6

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.742e0

QD
type: SiteQuality
SIO_000300: 1.68e0

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
all individuals: 48
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variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.92e0

MQRankSum
type: SiteQuality
SIO_000300: -5.76e-1

MQ
type: SiteQuality
SIO_000300: 5.88e1

QD
type: SiteQuality
SIO_000300: 9.84e0

FS
type: SiteQuality
SIO_000300: 1.998e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 2.135095e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

GenotypeQuality
all individuals: 130
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3179
bin: 7.75e1
variant carriers: 10

Latino
type: Population
allele count: 7
allele frequency: 6.080611535788742e-4
allele num: 11512
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.984866123399302e-4
allele num: 8590
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.587155963302753e-3
allele num: 872
num of homozygotes: 0

African
type: Population
allele count: 59
allele frequency: 6.159949885153477e-3
allele num: 9578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 165
allele frequency: 2.559409319352237e-3
allele num: 64468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 30
allele frequency: 4.787743376954996e-3
allele num: 6266
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.908e1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.5e-1

FS
type: SiteQuality
SIO_000300: 2.67648e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.16e-2

ClippingRankSum
type: SiteQuality
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DP
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.975e0

ReadPosRankSum
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SIO_000300: -1.635e0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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African
type: Population
allele count: 0
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East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.017132551848512e-5
allele num: 66540
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
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South Asian
type: Population
allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: -7.4e-2

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.074992e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.21e-1

MQ
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SIO_000300: 5.884e1

FS
type: SiteQuality
SIO_000300: 1.106e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e-1

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502990951994469e-5
allele num: 66534
num of homozygotes: 0

South Asian
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East Asian
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

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

DP
type: SiteQuality
SIO_000300: 2.07443e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1610
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66460
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.1e1

DP
type: SiteQuality
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BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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MQ
type: SiteQuality
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MQRankSum
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SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.25e-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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bin: 2.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66434
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.072212e6

MQ
type: SiteQuality
SIO_000300: 5.896e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

QD
type: SiteQuality
SIO_000300: 1.267e1

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-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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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505751972535084e-5
allele num: 66412
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.35e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

FS
type: SiteQuality
SIO_000300: 1.778e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.071573e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.51e-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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505751972535084e-5
allele num: 66412
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

DP
type: SiteQuality
SIO_000300: 2.071573e6

VQSLOD
type: SiteQuality
SIO_000300: 7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.49e0

FS
type: SiteQuality
SIO_000300: 1.778e0

QD
type: SiteQuality
SIO_000300: 1.239e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.35e-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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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506205566935775e-5
allele num: 66392
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.74e0

FS
type: SiteQuality
SIO_000300: 9.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.723e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.786e0

DP
type: SiteQuality
SIO_000300: 2.070751e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.69e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506205566935775e-5
allele num: 66392
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

DP
type: SiteQuality
SIO_000300: 2.070628e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.516e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.069251e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507159005275056e-5
allele num: 66350
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

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

East 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: 2.43e0

FS
type: SiteQuality
SIO_000300: 4.22e-1

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.824e1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e0

VQSLOD
type: SiteQuality
SIO_000300: -1.631e0

GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.533776635937736e-5
allele num: 66170
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.83e-1

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.232e0

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.3e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.053268765133172e-5
allele num: 66080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.472e0

QD
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SIO_000300: 1.186e1

VQSLOD
type: SiteQuality
SIO_000300: 9.48e-1

DP
type: SiteQuality
SIO_000300: 2.059073e6

MQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.31e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519248883352071e-5
allele num: 65822
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.18e-1

FS
type: SiteQuality
SIO_000300: 3.307e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 2.047247e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.515e0

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

QD
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SIO_000300: 1.15e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-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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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

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

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

Latino
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allele count: 10
allele frequency: 8.658008658008658e-4
allele num: 11550
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65738
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.12e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 1.294e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

FS
type: SiteQuality
SIO_000300: 2.008e0

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e-1

DP
type: SiteQuality
SIO_000300: 2.042655e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
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: 1.543114622554163e-5
allele num: 64804
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16314
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.79e-1

FS
type: SiteQuality
SIO_000300: 4.501e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

QD
type: SiteQuality
SIO_000300: 1.114e1

DP
type: SiteQuality
SIO_000300: 1.947453e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.483e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-2

MQ
type: SiteQuality
SIO_000300: 5.869e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.481481481481481e-3
allele num: 2700
num of homozygotes: 0

African
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allele count: 1
allele frequency: 5.319148936170213e-3
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 9.328358208955224e-4
allele num: 7504
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 92
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 1.099e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.988e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.63e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

FS
type: SiteQuality
SIO_000300: 5.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 1.4783e5

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2700
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 188
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East Asian
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allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 2.664535038635758e-4
allele num: 7506
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.47425e5

MQ
type: SiteQuality
SIO_000300: 5.88e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.01e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.07e-1

VQSLOD
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BaseQRankSum
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SIO_000300: -1.879e0

FS
type: SiteQuality
SIO_000300: 5.919e0

QD
type: SiteQuality
SIO_000300: 6.8e0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Latino
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allele frequency: 1.08695652173913e-2
allele num: 92
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European (Finnish)
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allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2702
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 1.332267519317879e-4
allele num: 7506
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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FS
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BaseQRankSum
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ReadPosRankSum
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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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variant carriers: 0

South Asian
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allele frequency: 1.332622601279318e-4
allele num: 7504
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 2692
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 116
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European (Finnish)
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allele count: 0
allele frequency: NaN
allele num: 0
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QD
type: SiteQuality
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BaseQRankSum
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MQRankSum
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FS
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MQ
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

East Asian
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allele frequency: 2.833864682961389e-3
allele num: 5646
num of homozygotes: 0

South Asian
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allele num: 14582
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Other
type: Population
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African
type: Population
allele count: 3
allele frequency: 3.920543648719289e-4
allele num: 7652
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5772
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 54326
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e-1

FS
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QD
type: SiteQuality
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DP
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InbreedingCoeff
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SIO_000300: -2.9e-3

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 5.47e-1

MQRankSum
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SIO_000300: -3.47e-1

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 5.43931537150524e-5
allele num: 55154
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5872
num of homozygotes: 0

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

Latino
type: Population
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allele frequency: 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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Other
type: Population
allele count: 1
allele frequency: 1.213592233009709e-3
allele num: 824
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.28e1

MQ
type: SiteQuality
SIO_000300: 5.994e1

DP
type: SiteQuality
SIO_000300: 1.498081e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.95e-1

GenotypeQuality
all individuals: 103
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7437
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2488
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1537
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1892
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2285
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6404
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6040
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.248751248751249e-4
allele num: 8008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10938
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.315379163713678e-5
allele num: 56440
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.55339e6

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

QD
type: SiteQuality
SIO_000300: 1.59e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.65e-1

GenotypeQuality
all individuals: 2510
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29574
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9311
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 4106
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2720
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1753
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 7
allele frequency: 6.155469574393247e-4
allele num: 11372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7716
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61272
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

MQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.569e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

DP
type: SiteQuality
SIO_000300: 1.653955e6

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

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

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34641
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9311
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 955
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7746
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e-1

FS
type: SiteQuality
SIO_000300: 4.073e0

QD
type: SiteQuality
SIO_000300: 1.323e1

DP
type: SiteQuality
SIO_000300: 1.729624e6

MQRankSum
type: SiteQuality
SIO_000300: 8.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.647e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.83e-1

MQ
type: SiteQuality
SIO_000300: 5.886e1

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34645
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
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variant carriers: 0

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

GenotypeQuality
all individuals: 955
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7751
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9313
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 841
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.203e0

MQ
type: SiteQuality
SIO_000300: 5.916e1

DP
type: SiteQuality
SIO_000300: 1.729973e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.3e0

FS
type: SiteQuality
SIO_000300: 3.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.247e0

QD
type: SiteQuality
SIO_000300: 1.204e1

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

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

GenotypeQuality
all individuals: 2787
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34651
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 841
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1797
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997152704930316e-5
allele num: 66730
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.929e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.149e0

MQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

DP
type: SiteQuality
SIO_000300: 1.730145e6

VQSLOD
type: SiteQuality
SIO_000300: 4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.478e0

QD
type: SiteQuality
SIO_000300: 1.184e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

GenotypeQuality
all individuals: 841
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2594
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2787
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 34657
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7750
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.058e0

FS
type: SiteQuality
SIO_000300: 1.784e0

QD
type: SiteQuality
SIO_000300: 1.091e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.730194e6

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.83e0

VQSLOD
type: SiteQuality
SIO_000300: 6.36e-1

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

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 2779
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 953
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 115
allele frequency: 6.964631782945737e-3
allele num: 16512
num of homozygotes: 3

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.284e1

FS
type: SiteQuality
SIO_000300: 6.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.38e-2

MQ
type: SiteQuality
SIO_000300: 5.891e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.603e-1

DP
type: SiteQuality
SIO_000300: 1.739642e6

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

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

GenotypeQuality
all individuals: 7740
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34618
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9384
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2588
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.739642e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 1.284e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.603e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.53e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

FS
type: SiteQuality
SIO_000300: 6.05e-1

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 7757
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 954
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2591
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9322
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

South Asian
type: Population
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Latino
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
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FS
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MQ
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
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European (Non-Finnish)
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allele frequency: 1.498441620714457e-5
allele num: 66736
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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South Asian
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Latino
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allele num: 11576
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East Asian
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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FS
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MQ
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VQSLOD
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ReadPosRankSum
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16512
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Latino
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Other
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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allele frequency: 2.996883241428914e-5
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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FS
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VQSLOD
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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QD
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BaseQRankSum
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MQRankSum
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DP
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InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
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East Asian
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allele frequency: 0.0e0
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Latino
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Other
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498441620714457e-5
allele num: 66736
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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DP
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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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Latino
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allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

African
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South Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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allele frequency: 4.495324862143371e-5
allele num: 66736
num of homozygotes: 0

VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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QD
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DP
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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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South Asian
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East Asian
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Other
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Latino
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European (Non-Finnish)
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European (Finnish)
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African
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FS
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DP
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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Other
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European (Non-Finnish)
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South Asian
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African
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East Asian
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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InbreedingCoeff
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DP
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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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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East Asian
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Other
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European (Non-Finnish)
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South Asian
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European (Finnish)
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African
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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MQ
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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European (Non-Finnish)
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European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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DP
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ReadPosRankSum
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele num: 11556
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African
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DP
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FS
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MQRankSum
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BaseQRankSum
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele num: 10386
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European (Finnish)
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allele frequency: 0.0e0
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Other
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South Asian
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East Asian
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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FS
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MQRankSum
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VQSLOD
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DP
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 3.484320557491289e-4
allele num: 8610
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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MQRankSum
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DP
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FS
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ClippingRankSum
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MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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Other
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South Asian
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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QD
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DP
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FS
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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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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South Asian
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East Asian
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African
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
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QD
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