11-7647079-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647079
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647079
    reference: chr 11
allele count: 2
allele frequency: 1.652510162937502e-5
allele num: 121028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29566C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.309C>G
  hgvsp: ENST00000533792.1:c.309C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.447C>G
  hgvsp: ENST00000528883.1:c.447C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.309C>G
  hgvsp: ENST00000529575.1:c.309C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.354C>G
  hgvsp: ENST00000530181.1:c.354C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.783C>G
  hgvsp: ENST00000299492.4:c.783C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15426C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.38C>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8013
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu261Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-7647081-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647081
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647081
    reference: chr 11
allele count: 1
allele frequency: 8.267469162340024e-6
allele num: 120956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.356C>G
  hgvsp: ENSP00000437321.1:p.Ser119Cys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29564C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.311C>G
  hgvsp: ENSP00000436498.1:p.Ser104Cys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.449C>G
  hgvsp: ENSP00000435469.1:p.Ser150Cys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.785C>G
  hgvsp: ENSP00000299492.4:p.Ser262Cys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15428C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.311C>G
  hgvsp: ENSP00000435794.1:p.Ser104Cys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.40C>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser262Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

11-7647083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647083
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647083
    reference: chr 11
allele count: 10
allele frequency: 8.278008642241022e-5
allele num: 120802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.358C>T
  hgvsp: ENSP00000437321.1:p.Arg120Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.42C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.313C>T
  hgvsp: ENSP00000436498.1:p.Arg105Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.313C>T
  hgvsp: ENSP00000435794.1:p.Arg105Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.451C>T
  hgvsp: ENSP00000435469.1:p.Arg151Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15430C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.787C>T
  hgvsp: ENSP00000299492.4:p.Arg263Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29562C>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27500
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7947
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1750
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg263Trp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-7647084-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647084
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647084
    reference: chr 11
allele count: 1
allele frequency: 8.276638360563474e-6
allele num: 120822
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.788G>A
  hgvsp: ENSP00000299492.4:p.Arg263Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.359G>A
  hgvsp: ENSP00000437321.1:p.Arg120Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.314G>A
  hgvsp: ENSP00000435794.1:p.Arg105Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.314G>A
  hgvsp: ENSP00000436498.1:p.Arg105Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.452G>A
  hgvsp: ENSP00000435469.1:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29561G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.43G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15431G>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2896
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg263Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP

11-7647092-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647092
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647092
    reference: chr 11
allele count: 1
allele frequency: 8.305647840531562e-6
allele num: 120400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.322G>A
  hgvsp: ENSP00000435794.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.322G>A
  hgvsp: ENSP00000436498.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.796G>A
  hgvsp: ENSP00000299492.4:p.Ala266Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15439G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29553G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.367G>A
  hgvsp: ENSP00000437321.1:p.Ala123Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.460G>A
  hgvsp: ENSP00000435469.1:p.Ala154Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.51G>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7858
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43778
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala266Thr
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ

11-7647092-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647092
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647092
    reference: chr 11
allele count: 2
allele frequency: 1.661129568106312e-5
allele num: 120400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.367G>C
  hgvsp: ENSP00000437321.1:p.Ala123Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.322G>C
  hgvsp: ENSP00000436498.1:p.Ala108Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.796G>C
  hgvsp: ENSP00000299492.4:p.Ala266Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.460G>C
  hgvsp: ENSP00000435469.1:p.Ala154Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29553G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.51G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.322G>C
  hgvsp: ENSP00000435794.1:p.Ala108Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15439G>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27411
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala266Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ

11-7647096-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647096
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647096
    reference: chr 11
allele count: 1
allele frequency: 8.324592511196577e-6
allele num: 120126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.464T>C
  hgvsp: ENSP00000435469.1:p.Leu155Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.800T>C
  hgvsp: ENSP00000299492.4:p.Leu267Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.326T>C
  hgvsp: ENSP00000436498.1:p.Leu109Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.326T>C
  hgvsp: ENSP00000435794.1:p.Leu109Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15443T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29549T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.371T>C
  hgvsp: ENSP00000437321.1:p.Leu124Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.55T>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20038
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1710
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu267Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-7647098-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647098
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647098
    reference: chr 11
allele count: 364
allele frequency: 3.035863219349458e-3
allele num: 119900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.328C>T
  hgvsp: ENSP00000436498.1:p.His110Tyr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.328C>T
  hgvsp: ENSP00000435794.1:p.His110Tyr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.57C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15445C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.802C>T
  hgvsp: ENSP00000299492.4:p.His268Tyr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.373C>T
  hgvsp: ENSP00000437321.1:p.His125Tyr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.466C>T
  hgvsp: ENSP00000435469.1:p.His156Tyr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29547C>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 27157
  bin: 2.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 3.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19772
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7406
  bin: 3.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43183
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His268Tyr
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

11-7647120-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647120
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647120
    reference: chr 11
allele count: 2
allele frequency: 1.740583443570285e-5
allele num: 114904
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.395G>C
  hgvsp: ENSP00000437321.1:p.Arg132Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.488G>C
  hgvsp: ENSP00000435469.1:p.Arg163Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.824G>C
  hgvsp: ENSP00000299492.4:p.Arg275Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29525G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.350G>C
  hgvsp: ENSP00000435794.1:p.Arg117Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15467G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.79G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.350G>C
  hgvsp: ENSP00000436498.1:p.Arg117Thr
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23787
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg275Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-7647121-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647121
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647121
    reference: chr 11
allele count: 2
allele frequency: 1.740977384703773e-5
allele num: 114878
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15468A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.825A>G
  hgvsp: ENST00000299492.4:c.825A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.489A>G
  hgvsp: ENST00000528883.1:c.489A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.351A>G
  hgvsp: ENST00000533792.1:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.80A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29524A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.396A>G
  hgvsp: ENST00000530181.1:c.396A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.351A>G
  hgvsp: ENST00000529575.1:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23804
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1195
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
hgvs: c.825A>G
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

11-7647122-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647122
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647122
    reference: chr 11
allele count: 2
allele frequency: 1.745749100939213e-5
allele num: 114564
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.397G>C
  hgvsp: ENSP00000437321.1:p.Asp133His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.826G>C
  hgvsp: ENSP00000299492.4:p.Asp276His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.490G>C
  hgvsp: ENSP00000435469.1:p.Asp164His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.81G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.352G>C
  hgvsp: ENSP00000435794.1:p.Asp118His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29523G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.352G>C
  hgvsp: ENSP00000436498.1:p.Asp118His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15469G>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15831
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1285
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp276His
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-7647123-G-GTGACTAGCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647123
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647132
    reference: chr 11
allele count: 1
allele frequency: 8.76531739214277e-6
allele num: 114086
alternate allele: GTGACTAGCT
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: splice donor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15454
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6818
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
hgvs: c.826+7_826+15dupAGCTTGACT
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

11-7647126-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647126
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647126
    reference: chr 11
allele count: 1
allele frequency: 8.930644613928233e-6
allele num: 111974
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.352+4A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.397+4A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29519A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15473A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.826+4A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.81+4A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.490+4A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.352+4A>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2787
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11149
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
hgvs: c.826+4A>G
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

11-7647149-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647149
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647149
    reference: chr 11
allele count: 2
allele frequency: 1.927376455169224e-5
allele num: 103768
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.826+27C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.490+27C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29496C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.81+27C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.397+27C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15496C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.352+27C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.352+27C>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6729
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15014
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6117
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

11-7647154-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647154
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647154
    reference: chr 11
allele count: 2
allele frequency: 1.965563330450507e-5
allele num: 101752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.352+32G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.397+32G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.81+32G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15501G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29491G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.490+32G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.352+32G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.826+32G>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9267
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7170
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10984
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7404
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-7647159-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647159
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647159
    reference: chr 11
allele count: 2
allele frequency: 2.080213013812614e-5
allele num: 96144
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.490+37G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.81+37G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.352+37G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.397+37G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29486G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.352+37G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15506G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.826+37G>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6575
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5476
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

11-7647162-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647162
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647162
    reference: chr 11
allele count: 2
allele frequency: 2.099825714465699e-5
allele num: 95246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.352+40C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.81+40C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.826+40C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29483C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15509C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.397+40C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.352+40C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.490+40C>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12871
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21968
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18506
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6390
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1572
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5923
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-7647163-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647163
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647163
    reference: chr 11
allele count: 2
allele frequency: 2.127976507139361e-5
allele num: 93986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.352+41C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29482C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.352+41C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.397+41C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15510C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.826+41C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.490+41C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.81+41C>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13238
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4528
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5806
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1968
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

11-7647173-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7647173
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7647173
    reference: chr 11
allele count: 1
allele frequency: 1.148079263392345e-5
allele num: 87102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-29472C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.352+51C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.490+51C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.826+51C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.352+51C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.81+51C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.397+51C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+15520C>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19718
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5917
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3022
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2355
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5827
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3056
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

11-7649474-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649474
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649474
    reference: chr 11
allele count: 14
allele frequency: 1.297882597248489e-4
allele num: 107868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.398-42G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27171G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.353-42G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.82-42G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.827-42G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17821G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.353-42G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.491-42G>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10024
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15372
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4196
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5523
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7186
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3066
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2520
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4857
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

11-7649481-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649481
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649481
    reference: chr 11
allele count: 1
allele frequency: 9.181387491277682e-6
allele num: 108916
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.398-35T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17828T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27164T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.827-35T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.82-35T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.353-35T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.491-35T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.353-35T>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5492
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17878
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

11-7649493-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649493
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649493
    reference: chr 11
allele count: 1
allele frequency: 8.570449091532397e-6
allele num: 116680
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.82-23T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.827-23T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.491-23T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17840T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.353-23T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.353-23T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27152T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.398-23T>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

11-7649498-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649498
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649498
    reference: chr 11
allele count: 2
allele frequency: 1.673556139440698e-5
allele num: 119506
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.398-18A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.353-18A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.827-18A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.353-18A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27147A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.491-18A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17845A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.82-18A>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1661
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3696
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

11-7649500-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649500
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649500
    reference: chr 11
allele count: 85
allele frequency: 7.077553331445986e-4
allele num: 120098
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.353-16A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27145A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.827-16A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17847A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.398-16A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.353-16A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.491-16A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.82-16A>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12060
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7872
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2866
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9629
  bin: 9.75e1
  variant carriers: 85
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

11-7649506-ATTCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649506
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649502
    reference: chr 11
allele count: 3
allele frequency: 2.482868209355447e-5
allele num: 120828
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.82-7_82-4delCTTT
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.398-7_398-4delCTTT
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.491-7_491-4delCTTT
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.827-7_827-4delCTTT
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17856_1097+17859delCTTT
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.353-7_353-4delCTTT
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.353-7_353-4delCTTT
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27136_317-27133delCTTT
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4476
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3751
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2894
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7571
  bin: 6.75e1
  variant carriers: 0
hgvs: c.827-7_827-4delCTTT
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: ATTCT
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

11-7649517-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649517
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649517
    reference: chr 11
allele count: 2
allele frequency: 1.650273945474949e-5
allele num: 121192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.83C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.492C>G
  hgvsp: ENSP00000435469.1:p.Asp164Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27128C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.354C>G
  hgvsp: ENSP00000436498.1:p.Asp118Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17864C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.828C>G
  hgvsp: ENSP00000299492.4:p.Asp276Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.399C>G
  hgvsp: ENSP00000437321.1:p.Asp133Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.354C>G
  hgvsp: ENSP00000435794.1:p.Asp118Glu
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1682
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp276Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

11-7649518-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649518
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649518
    reference: chr 11
allele count: 5
allele frequency: 4.124936063491016e-5
allele num: 121214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17865C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.84C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27127C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.355C>G
  hgvsp: ENSP00000435794.1:p.Gln119Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.493C>G
  hgvsp: ENSP00000435469.1:p.Gln165Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.355C>G
  hgvsp: ENSP00000436498.1:p.Gln119Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.400C>G
  hgvsp: ENSP00000437321.1:p.Gln134Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.829C>G
  hgvsp: ENSP00000299492.4:p.Gln277Glu
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2905
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln277Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

11-7649526-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649526
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649526
    reference: chr 11
allele count: 8
allele frequency: 6.595435958316844e-5
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.363T>G
  hgvsp: ENSP00000435794.1:p.Ile121Met
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.92T>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.837T>G
  hgvsp: ENSP00000299492.4:p.Ile279Met
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.408T>G
  hgvsp: ENSP00000437321.1:p.Ile136Met
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17873T>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.501T>G
  hgvsp: ENSP00000435469.1:p.Ile167Met
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27119T>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.363T>G
  hgvsp: ENSP00000436498.1:p.Ile121Met
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3757
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2704
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4485
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile279Met
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

11-7649531-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649531
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649531
    reference: chr 11
allele count: 390
allele frequency: 3.214427007780562e-3
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.506G>A
  hgvsp: ENSP00000435469.1:p.Arg169His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.97G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.842G>A
  hgvsp: ENSP00000299492.4:p.Arg281His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.368G>A
  hgvsp: ENSP00000435794.1:p.Arg123His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27114G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.413G>A
  hgvsp: ENSP00000437321.1:p.Arg138His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.368G>A
  hgvsp: ENSP00000436498.1:p.Arg123His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17878G>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 9.75e1
  variant carriers: 214
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 12295
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  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: 8
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg281His
num of homozygotes: 10
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

11-7649541-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649541
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649541
    reference: chr 11
allele count: 2
allele frequency: 1.648043772042586e-5
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.378G>A
  hgvsp: ENSP00000436498.1:p.Met126Ile
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.378G>A
  hgvsp: ENSP00000435794.1:p.Met126Ile
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.423G>A
  hgvsp: ENSP00000437321.1:p.Met141Ile
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.107G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.852G>A
  hgvsp: ENSP00000299492.4:p.Met284Ile
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.516G>A
  hgvsp: ENSP00000435469.1:p.Met172Ile
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17888G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27104G>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7974
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27690
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7560
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met284Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

11-7649556-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649556
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649556
    reference: chr 11
allele count: 3
allele frequency: 2.471943441934048e-5
allele num: 121362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27089G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.531G>C
  hgvsp: ENSP00000435469.1:p.Leu177Phe
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.867G>C
  hgvsp: ENSP00000299492.4:p.Leu289Phe
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.393G>C
  hgvsp: ENSP00000435794.1:p.Leu131Phe
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.438G>C
  hgvsp: ENSP00000437321.1:p.Leu146Phe
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17903G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.393G>C
  hgvsp: ENSP00000436498.1:p.Leu131Phe
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.122G>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3747
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu289Phe
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: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-7649558-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649558
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649558
    reference: chr 11
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.533T>C
  hgvsp: ENSP00000435469.1:p.Leu178Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.440T>C
  hgvsp: ENSP00000437321.1:p.Leu147Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.124T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17905T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.395T>C
  hgvsp: ENSP00000435794.1:p.Leu132Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.869T>C
  hgvsp: ENSP00000299492.4:p.Leu290Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.395T>C
  hgvsp: ENSP00000436498.1:p.Leu132Pro
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27087T>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7563
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3748
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu290Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

11-7649583-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649583
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649583
    reference: chr 11
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+6A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+6A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27062A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17930A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+6A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+6A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+6A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+6A>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9912
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4465
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7551
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: c.888+6A>G
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

11-7649586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649586
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649586
    reference: chr 11
allele count: 102
allele frequency: 8.409458167067903e-4
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+9G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+9G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27059G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+9G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+9G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17933G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+9G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+9G>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29585
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7988
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12307
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10008
  bin: 9.75e1
  variant carriers: 100
num of homozygotes: 2
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

11-7649588-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649588
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649588
    reference: chr 11
allele count: 2
allele frequency: 1.649130908011478e-5
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+11C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27057C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17935C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+11C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+11C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+11C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+11C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+11C>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7990
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1682
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2700
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27295
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

11-7649589-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649589
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649589
    reference: chr 11
allele count: 14
allele frequency: 1.154353562005277e-4
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17936A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+12A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27056A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+12A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+12A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+12A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+12A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+12A>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4250
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9956
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 2897
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4461
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  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: A
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

11-7649593-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649593
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649593
    reference: chr 11
allele count: 21
allele frequency: 1.731844496857939e-4
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+16G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17940G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+16G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+16G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+16G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27052G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+16G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+16G>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4460
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27155
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

11-7649607-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649607
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649607
    reference: chr 11
allele count: 7
allele frequency: 5.775672865888876e-5
allele num: 121198
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+30T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27038T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+30T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+30T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+30T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+30T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+30T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17954T>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26230
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2890
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

11-7649609-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649609
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649609
    reference: chr 11
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+32C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+32C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+32C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27036C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17956C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+32C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+32C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+32C>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-7649614-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649614
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649614
    reference: chr 11
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+37C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17961C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+37C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+37C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+37C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+37C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+37C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27031C>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4248
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2889
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7441
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4447
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-7649618-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649618
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649618
    reference: chr 11
allele count: 2
allele frequency: 1.652155236506022e-5
allele num: 121054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+41C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+41C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+41C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17965C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+41C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+41C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+41C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27027C>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7446
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25170
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/11-7649619-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649619
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649619
    reference: chr 11
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+42A>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+42A>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+42A>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+42A>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27026A>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+42A>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17966A>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+42A>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9984
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

11-7649619-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649619
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649619
    reference: chr 11
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+42A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+42A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+42A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27026A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+42A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+42A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+42A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17966A>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-7649621-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649621
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649621
    reference: chr 11
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+44C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+44C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+44C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17968C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+44C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+44C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27024C>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+44C>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3753
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7436
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

11-7649625-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649625
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649625
    reference: chr 11
allele count: 2
allele frequency: 1.652373634726284e-5
allele num: 121038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+48G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+48G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27020G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17972G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+48G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+48G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+48G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+48G>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7975
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4461
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7432
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

11-7649629-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7649629
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7649629
    reference: chr 11
allele count: 1
allele frequency: 8.263097008758882e-6
allele num: 121020
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.888+52G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-27016G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.459+52G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.414+52G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.143+52G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.552+52G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.414+52G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+17976G>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2711
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7465
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

11-7650646-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650646
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650646
    reference: chr 11
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-44T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-44T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-44T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-44T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+18993T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25999T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-44T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-44T>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3844
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12210
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4271
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5516
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-7650651-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650651
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650651
    reference: chr 11
allele count: 6
allele frequency: 4.948616861587186e-5
allele num: 121246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-39G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-39G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-39G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-39G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25994G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-39G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+18998G>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-39G>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4236
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2573
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

11-7650653-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650653
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650653
    reference: chr 11
allele count: 4
allele frequency: 3.298588204248581e-5
allele num: 121264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-37A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-37A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25992A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-37A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-37A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19000A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-37A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-37A>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7738
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12617
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-7650655-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650655
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650655
    reference: chr 11
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-35A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-35A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-35A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25990A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-35A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-35A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19002A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-35A>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5529
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26117
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

11-7650666-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650666
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650666
    reference: chr 11
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-24A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25979A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19013A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-24A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-24A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-24A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-24A>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-24A>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12913
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-7650671-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650671
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650671
    reference: chr 11
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19018T>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-19T>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-19T>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25974T>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-19T>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-19T>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-19T>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-19T>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12958
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3174
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-7650674-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650674
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650674
    reference: chr 11
allele count: 4
allele frequency: 3.297554863069035e-5
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-16A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-16A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-16A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25971A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-16A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-16A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-16A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19021A>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2600
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5561
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3850
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

11-7650676-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650676
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650676
    reference: chr 11
allele count: 2
allele frequency: 1.64866870002473e-5
allele num: 121310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-14T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25969T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-14T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-14T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-14T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19023T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-14T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-14T>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5563
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

11-7650678-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650678
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650678
    reference: chr 11
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19025G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25967G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-12G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-12G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-12G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-12G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-12G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-12G>A
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2602
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

11-7650678-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650678
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650678
    reference: chr 11
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-12G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-12G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-12G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25967G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-12G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19025G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-12G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-12G>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4246
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

11-7650679-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650679
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650679
    reference: chr 11
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-11C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-11C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-11C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-11C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-11C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25966C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19026C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-11C>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6092
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3174
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26114
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2002
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5566
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

11-7650683-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650683
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650683
    reference: chr 11
allele count: 5
allele frequency: 4.121196135966503e-5
allele num: 121324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.415-7A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.460-7A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.144-7A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.553-7A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.415-7A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19030A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25962A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.889-7A>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5562
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26112
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
hgvs: c.889-7A>G
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

11-7650693-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650693
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650693
    reference: chr 11
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.418C>T
  hgvsp: ENSP00000435794.1:p.Arg140Cys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.892C>T
  hgvsp: ENSP00000299492.4:p.Arg298Cys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.556C>T
  hgvsp: ENSP00000435469.1:p.Arg186Cys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.418C>T
  hgvsp: ENSP00000436498.1:p.Arg140Cys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25952C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.463C>T
  hgvsp: ENSP00000437321.1:p.Arg155Cys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19040C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.147C>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3852
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12980
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg298Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

11-7650694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650694
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650694
    reference: chr 11
allele count: 4
allele frequency: 3.296522169111587e-5
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.557G>A
  hgvsp: ENSP00000435469.1:p.Arg186His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.419G>A
  hgvsp: ENSP00000435794.1:p.Arg140His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.464G>A
  hgvsp: ENSP00000437321.1:p.Arg155His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.419G>A
  hgvsp: ENSP00000436498.1:p.Arg140His
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25951G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19041G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.148G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.893G>A
  hgvsp: ENSP00000299492.4:p.Arg298His
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3851
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3173
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg298His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-7650696-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650696
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650696
    reference: chr 11
allele count: 2
allele frequency: 1.648342591524222e-5
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25949C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.895C>T
  hgvsp: ENSP00000299492.4:p.Arg299Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.421C>T
  hgvsp: ENSP00000436498.1:p.Arg141Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.559C>T
  hgvsp: ENSP00000435469.1:p.Arg187Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.466C>T
  hgvsp: ENSP00000437321.1:p.Arg156Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.150C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19043C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.421C>T
  hgvsp: ENSP00000435794.1:p.Arg141Trp
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4235
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26101
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg299Trp
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

11-7650697-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650697
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650697
    reference: chr 11
allele count: 6
allele frequency: 4.944620253164557e-5
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25948G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19044G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.422G>A
  hgvsp: ENSP00000435794.1:p.Arg141Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.560G>A
  hgvsp: ENSP00000435469.1:p.Arg187Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.151G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.467G>A
  hgvsp: ENSP00000437321.1:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.422G>A
  hgvsp: ENSP00000436498.1:p.Arg141Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.896G>A
  hgvsp: ENSP00000299492.4:p.Arg299Gln
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10364
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3851
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26103
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4234
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5554
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg299Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

11-7650700-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650700
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650700
    reference: chr 11
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.563T>C
  hgvsp: ENSP00000435469.1:p.Ile188Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.425T>C
  hgvsp: ENSP00000435794.1:p.Ile142Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25945T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.425T>C
  hgvsp: ENSP00000436498.1:p.Ile142Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.470T>C
  hgvsp: ENSP00000437321.1:p.Ile157Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.899T>C
  hgvsp: ENSP00000299492.4:p.Ile300Thr
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19047T>C
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.154T>C
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13042
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3854
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2004
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile300Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

11-7650712-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650712
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650712
    reference: chr 11
allele count: 3
allele frequency: 2.472024918011174e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19059C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.482C>T
  hgvsp: ENSP00000437321.1:p.Thr161Met
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.166C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25933C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.575C>T
  hgvsp: ENSP00000435469.1:p.Thr192Met
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.437C>T
  hgvsp: ENSP00000436498.1:p.Thr146Met
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.911C>T
  hgvsp: ENSP00000299492.4:p.Thr304Met
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.437C>T
  hgvsp: ENSP00000435794.1:p.Thr146Met
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5573
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26102
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr304Met
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

11-7650713-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650713
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650713
    reference: chr 11
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.438G>A
  hgvsp: ENST00000533792.1:c.438G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.483G>A
  hgvsp: ENST00000530181.1:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.912G>A
  hgvsp: ENST00000299492.4:c.912G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25932G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.167G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.576G>A
  hgvsp: ENST00000528883.1:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19060G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.438G>A
  hgvsp: ENST00000529575.1:c.438G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13070
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3175
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr304Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

11-7650716-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650716
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650716
    reference: chr 11
allele count: 2
allele frequency: 1.648043772042586e-5
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25929G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.579G>T
  hgvsp: ENST00000528883.1:c.579G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.486G>T
  hgvsp: ENST00000530181.1:c.486G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.915G>T
  hgvsp: ENST00000299492.4:c.915G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.170G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.441G>T
  hgvsp: ENST00000529575.1:c.441G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19063G>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.441G>T
  hgvsp: ENST00000533792.1:c.441G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26099
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2007
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3856
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4245
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly305Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

11-7650724-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650724
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650724
    reference: chr 11
allele count: 3
allele frequency: 2.472024918011174e-5
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25921A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.587A>G
  hgvsp: ENSP00000435469.1:p.Asn196Ser
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.449A>G
  hgvsp: ENSP00000436498.1:p.Asn150Ser
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.923A>G
  hgvsp: ENSP00000299492.4:p.Asn308Ser
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19071A>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.449A>G
  hgvsp: ENSP00000435794.1:p.Asn150Ser
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.494A>G
  hgvsp: ENSP00000437321.1:p.Asn165Ser
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.178A>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2607
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2007
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn308Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

11-7650725-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650725
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650725
    reference: chr 11
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19072C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.495C>G
  hgvsp: ENSP00000437321.1:p.Asn165Lys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.588C>G
  hgvsp: ENSP00000435469.1:p.Asn196Lys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.179C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25920C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.924C>G
  hgvsp: ENSP00000299492.4:p.Asn308Lys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.450C>G
  hgvsp: ENSP00000435794.1:p.Asn150Lys
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.450C>G
  hgvsp: ENSP00000436498.1:p.Asn150Lys
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11222
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4246
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13080
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2007
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn308Lys
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

11-7650726-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650726
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650726
    reference: chr 11
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.589C>G
  hgvsp: ENSP00000435469.1:p.Gln197Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25919C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.925C>G
  hgvsp: ENSP00000299492.4:p.Gln309Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.496C>G
  hgvsp: ENSP00000437321.1:p.Gln166Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.451C>G
  hgvsp: ENSP00000435794.1:p.Gln151Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19073C>G
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.451C>G
  hgvsp: ENSP00000436498.1:p.Gln151Glu
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.180C>G
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5574
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2606
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln309Glu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

11-7650732-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650732
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650732
    reference: chr 11
allele count: 3
allele frequency: 2.471943441934048e-5
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.457C>T
  hgvsp: ENSP00000435794.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19079C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.502C>T
  hgvsp: ENSP00000437321.1:p.Arg168Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.931C>T
  hgvsp: ENSP00000299492.4:p.Arg311Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.457C>T
  hgvsp: ENSP00000436498.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.186C>T
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.595C>T
  hgvsp: ENSP00000435469.1:p.Arg199Trp
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25913C>T
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26096
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5571
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2607
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg311Trp
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

11-7650733-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7650733
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 7650733
    reference: chr 11
allele count: 3
allele frequency: 2.471984179301253e-5
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532926
  gene symbol: PPFIBP2
  hgvsc: ENST00000532926.1:n.1097+19080G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000299492
  ensembl transcript: ENST00000299492
  gene symbol: PPFIBP2
  hgvsc: ENST00000299492.4:c.932G>A
  hgvsp: ENSP00000299492.4:p.Arg311Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000436498
  ensembl transcript: ENST00000533792
  gene symbol: PPFIBP2
  hgvsc: ENST00000533792.1:c.458G>A
  hgvsp: ENSP00000436498.1:p.Arg153Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435794
  ensembl transcript: ENST00000529575
  gene symbol: PPFIBP2
  hgvsc: ENST00000529575.1:c.458G>A
  hgvsp: ENSP00000435794.1:p.Arg153Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000532416
  gene symbol: PPFIBP2
  hgvsc: ENST00000532416.1:n.187G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000437321
  ensembl transcript: ENST00000530181
  gene symbol: PPFIBP2
  hgvsc: ENST00000530181.1:c.503G>A
  hgvsp: ENSP00000437321.1:p.Arg168Gln
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166387
  ensembl transcript: ENST00000529021
  gene symbol: PPFIBP2
  hgvsc: ENST00000529021.1:n.317-25912G>A
  variant of: http://identifiers.org/hgnc/9250
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166387
  ensembl protein: ENSP00000435469
  ensembl transcript: ENST00000528883
  gene symbol: PPFIBP2
  hgvsc: ENST00000528883.1:c.596G>A
  hgvsp: ENSP00000435469.1:p.Arg199Gln
  variant of: http://identifiers.org/hgnc/9250
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg311Gln
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 88
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1790
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 285
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44575
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.646922631680494e-5
allele num: 10366
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.877e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.81e-1

FS
type: SiteQuality
SIO_000300: 1.215e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

DP
type: SiteQuality
SIO_000300: 1.675109e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

QD
type: SiteQuality
SIO_000300: 8.01e0

GenotypeQuality
all individuals: 231
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8003
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variant carriers: 0

GenotypeQuality
all individuals: 2904
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503578516870151e-5
allele num: 66508
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

FS
type: SiteQuality
SIO_000300: 1.3264e1

MQ
type: SiteQuality
SIO_000300: 5.877e1

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

QD
type: SiteQuality
SIO_000300: 9.35e0

VQSLOD
type: SiteQuality
SIO_000300: -2.188e0

DP
type: SiteQuality
SIO_000300: 1.674291e6

GenotypeQuality
all individuals: 613
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
all individuals: 278
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variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.219363492257042e-4
allele num: 16402
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.734906315058987e-4
allele num: 11528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.032335762028061e-5
allele num: 66428
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 9.48e-1

FS
type: SiteQuality
SIO_000300: 2.212e0

QD
type: SiteQuality
SIO_000300: 1.854e1

VQSLOD
type: SiteQuality
SIO_000300: 3.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-1

DP
type: SiteQuality
SIO_000300: 1.673468e6

GenotypeQuality
all individuals: 614
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 44380
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505117399157134e-5
allele num: 66440
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.07e-1

QD
type: SiteQuality
SIO_000300: 1.041e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.782e0

DP
type: SiteQuality
SIO_000300: 1.672507e6

GenotypeQuality
all individuals: 2900
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1729
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 940
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 206
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1443
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variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66234
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.12294881214793e-5
allele num: 16332
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.664387e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.68e-1

QD
type: SiteQuality
SIO_000300: 1.128e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.08e-1

FS
type: SiteQuality
SIO_000300: 1.998e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

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

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

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 275
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GenotypeQuality
all individuals: 111
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GenotypeQuality
all individuals: 43778
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variant carriers: 0

GenotypeQuality
all individuals: 940
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
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GenotypeQuality
all individuals: 1729
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 603
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variant carriers: 0

GenotypeQuality
all individuals: 7858
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2900
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.019597185735423e-5
allele num: 66234
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: 11496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

QD
type: SiteQuality
SIO_000300: 1.128e1

DP
type: SiteQuality
SIO_000300: 1.664387e6

FS
type: SiteQuality
SIO_000300: 1.998e0

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

GenotypeQuality
all individuals: 195
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 4
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GenotypeQuality
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GenotypeQuality
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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: 2897
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 604
bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16292
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.738994935722633e-5
allele num: 10268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66084
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.63e-1

FS
type: SiteQuality
SIO_000300: 3.183e0

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

QD
type: SiteQuality
SIO_000300: 9.98e0

DP
type: SiteQuality
SIO_000300: 1.659491e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

GenotypeQuality
all individuals: 250
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 193
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variant carriers: 0

GenotypeQuality
all individuals: 219
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 141
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GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 362

GenotypeQuality
all individuals: 251
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GenotypeQuality
all individuals: 7715
bin: 6.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 10
allele frequency: 1.527650473571647e-3
allele num: 6546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.13418251614029e-3
allele num: 11462
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.910068426197458e-4
allele num: 10230
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.348214285714286e-3
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 262
allele frequency: 3.971983869500622e-3
allele num: 65962
num of homozygotes: 0

South Asian
type: Population
allele count: 72
allele frequency: 4.430769230769231e-3
allele num: 16250
num of homozygotes: 1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.722e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

FS
type: SiteQuality
SIO_000300: 1.389e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.39e0

QD
type: SiteQuality
SIO_000300: 1.258e1

DP
type: SiteQuality
SIO_000300: 1.661721e6

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 36598
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10916
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.279099513942185e-4
allele num: 15636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63294
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.734e1

MQ
type: SiteQuality
SIO_000300: 5.913e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.445e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.42e-1

DP
type: SiteQuality
SIO_000300: 1.53719e6

GenotypeQuality
all individuals: 1107
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2792
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variant carriers: 2

GenotypeQuality
all individuals: 229
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GenotypeQuality
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63278
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.27959053103007e-4
allele num: 15630
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.909e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

QD
type: SiteQuality
SIO_000300: 1.784e1

DP
type: SiteQuality
SIO_000300: 1.536798e6

VQSLOD
type: SiteQuality
SIO_000300: -9.729e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.169672572823227e-5
allele num: 63098
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15602
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10870
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.333e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.528062e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

FS
type: SiteQuality
SIO_000300: 4.097e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.171e0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10814
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.591647036353218e-5
allele num: 62828
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15562
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.985e-1

DP
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SIO_000300: 1.514779e6

MQ
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SIO_000300: 5.52e1

ClippingRankSum
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SIO_000300: -1.247e0

MQRankSum
type: SiteQuality
SIO_000300: -2.306e0

QD
type: SiteQuality
SIO_000300: 4.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.457e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6214
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.621323648626739e-5
allele num: 61678
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7758
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9580
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.377e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.863e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

QD
type: SiteQuality
SIO_000300: 1.174e1

DP
type: SiteQuality
SIO_000300: 1.443712e6

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6914
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.244668911335578e-4
allele num: 8910
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5956
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57166
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

FS
type: SiteQuality
SIO_000300: 7.284e0

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

DP
type: SiteQuality
SIO_000300: 1.153327e6

QD
type: SiteQuality
SIO_000300: 1.165e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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: 2

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8778
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.570153516601214e-5
allele num: 56020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5884
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.863e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.393e1

VQSLOD
type: SiteQuality
SIO_000300: -9.67e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.091645e6

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.892577311783187e-5
allele num: 52838
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

MQ
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -2.638e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.022884e6

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: 1

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5676
num of homozygotes: 0

Latino
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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.818834491713129e-5
allele num: 52372
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6016
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South Asian
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

VQSLOD
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BaseQRankSum
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.011084e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
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Latino
type: Population
allele count: 2
allele frequency: 2.378121284185493e-4
allele num: 8410
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 51608
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 720
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South Asian
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allele num: 13528
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-2

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.61e-1

FS
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

DP
type: SiteQuality
SIO_000300: 1.001262e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.086550098067855e-5
allele num: 47926
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12784
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

QD
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SIO_000300: 1.433e1

VQSLOD
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SIO_000300: 1.69e0

FS
type: SiteQuality
SIO_000300: 3.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 9.74758e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

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: 14

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7022
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Other
type: Population
allele count: 2
allele frequency: 2.298850574712644e-3
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59232
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 8.183306055646482e-4
allele num: 14664
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.004e1

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.534e0

VQSLOD
type: SiteQuality
SIO_000300: 3.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.519679e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.149425287356322e-3
allele num: 870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7178
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59810
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.641e1

MQRankSum
type: SiteQuality
SIO_000300: -1.613e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.123e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.575292e6

GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562011871290222e-5
allele num: 64020
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.684088e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.34e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

QD
type: SiteQuality
SIO_000300: 1.491e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9978
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.732801940738174e-4
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65808
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
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: 6572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16110
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.242e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.22e0

VQSLOD
type: SiteQuality
SIO_000300: 2.39e-1

QD
type: SiteQuality
SIO_000300: 1.504e1

FS
type: SiteQuality
SIO_000300: 8.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.18e-1

DP
type: SiteQuality
SIO_000300: 1.712915e6

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.732501732501733e-4
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511441613010489e-5
allele num: 66162
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

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

African
type: Population
allele count: 81
allele frequency: 8.027750247770069e-3
allele num: 10090
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.12e0

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.338e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.721783e6

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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bin: 3.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.927971891469842e-4
allele num: 10246
num of homozygotes: 0

Latino
type: Population
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
allele num: 66514
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.83e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.792e1

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.041e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.88e-1

DP
type: SiteQuality
SIO_000300: 1.730718e6

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 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: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001380635092142e-5
allele num: 66636
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.694e1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.985e1

FS
type: SiteQuality
SIO_000300: 1.352e1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.735032e6

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.817883985353633e-4
allele num: 10378
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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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
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
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European (Non-Finnish)
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allele count: 7
allele frequency: 1.049790041991602e-4
allele num: 66680
num of homozygotes: 0

MQ
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SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 3.12e0

MQRankSum
type: SiteQuality
SIO_000300: 5.11e-1

ClippingRankSum
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SIO_000300: -3.9e-1

BaseQRankSum
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SIO_000300: 4.64e0

ReadPosRankSum
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DP
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

Latino
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allele count: 15
allele frequency: 1.296456352636128e-3
allele num: 11570
num of homozygotes: 0

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

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

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

African
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allele count: 369
allele frequency: 3.546031135883145e-2
allele num: 10406
num of homozygotes: 10

European (Non-Finnish)
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allele count: 6
allele frequency: 8.995771987166032e-5
allele num: 66698
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 5.2e-2

VQSLOD
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FS
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SIO_000300: 6.4e-1

MQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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Latino
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allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -4.51e-1

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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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

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 (Non-Finnish)
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allele count: 3
allele frequency: 4.496807266840543e-5
allele num: 66714
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.37e-1

VQSLOD
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BaseQRankSum
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SIO_000300: -1.804e0

QD
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DP
type: SiteQuality
SIO_000300: 1.753799e6

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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QD
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SIO_000300: 1.35e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e-1

DP
type: SiteQuality
SIO_000300: 1.753683e6

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

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

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

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

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

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

Other
type: Population
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allele frequency: 1.101321585903084e-3
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African
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Latino
type: Population
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

South Asian
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allele count: 99
allele frequency: 6.017505470459519e-3
allele num: 16452
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DP
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QD
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BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

MQRankSum
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SIO_000300: 2.0e-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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European (Non-Finnish)
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allele count: 0
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num of homozygotes: 0

European (Finnish)
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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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Other
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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QD
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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African
type: Population
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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allele count: 14
allele frequency: 2.099643060679685e-4
allele num: 66678
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European (Finnish)
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FS
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DP
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QD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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BaseQRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 21

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
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: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
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: 19
allele frequency: 1.825869690563137e-3
allele num: 10406
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.269e1

MQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-1

FS
type: SiteQuality
SIO_000300: 2.571e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

DP
type: SiteQuality
SIO_000300: 1.754029e6

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 7476
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 5
allele frequency: 4.805843906189927e-4
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.092360180333861e-5
allele num: 16414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
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: 11572
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 3.26e0

DP
type: SiteQuality
SIO_000300: 1.747419e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.531e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 10
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variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 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: 66632
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.61e1

MQRankSum
type: SiteQuality
SIO_000300: -4.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.293e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.6608e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

DP
type: SiteQuality
SIO_000300: 1.74642e6

VQSLOD
type: SiteQuality
SIO_000300: -3.622e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 25403
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16334
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.07e-1

FS
type: SiteQuality
SIO_000300: 7.167e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.643e0

QD
type: SiteQuality
SIO_000300: 1.185e1

MQRankSum
type: SiteQuality
SIO_000300: -1.68e-1

DP
type: SiteQuality
SIO_000300: 1.744139e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e0

GenotypeQuality
all individuals: 2889
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4452
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1678
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 356
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GenotypeQuality
all individuals: 9982
bin: 9.75e1
variant carriers: 2

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
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: 2
allele frequency: 1.224739742804654e-4
allele num: 16330
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: 906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.391e0

QD
type: SiteQuality
SIO_000300: 1.218e1

VQSLOD
type: SiteQuality
SIO_000300: 5.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

FS
type: SiteQuality
SIO_000300: 4.221e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.38e-1

DP
type: SiteQuality
SIO_000300: 1.742965e6

MQ
type: SiteQuality
SIO_000300: 5.925e1

GenotypeQuality
all individuals: 305
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7455
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3750
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1678
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16352
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.913e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e-1

DP
type: SiteQuality
SIO_000300: 1.742492e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.12e0

MQRankSum
type: SiteQuality
SIO_000300: 2.14e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 5.45e-1

QD
type: SiteQuality
SIO_000300: 1.336e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

GenotypeQuality
all individuals: 305
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25106
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3750
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7455
bin: 6.75e1
variant carriers: 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: 906
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
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: 16352
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.913e0

QD
type: SiteQuality
SIO_000300: 1.336e1

VQSLOD
type: SiteQuality
SIO_000300: 5.45e-1

DP
type: SiteQuality
SIO_000300: 1.742492e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.12e0

MQRankSum
type: SiteQuality
SIO_000300: 2.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-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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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16328
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: 11568
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.16e-1

FS
type: SiteQuality
SIO_000300: 8.65e-1

DP
type: SiteQuality
SIO_000300: 1.742697e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.62e-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
all individuals: 2702
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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
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African
type: Population
allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

BaseQRankSum
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SIO_000300: -7.83e-1

FS
type: SiteQuality
SIO_000300: 7.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 1.743478e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-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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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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

South Asian
type: Population
allele count: 1
allele frequency: 6.130456105934282e-5
allele num: 16312
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.744916e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.924e1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

FS
type: SiteQuality
SIO_000300: 2.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.944e0

QD
type: SiteQuality
SIO_000300: 1.345e1

GenotypeQuality
all individuals: 98
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
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: 11538
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.03e-1

DP
type: SiteQuality
SIO_000300: 2.72244e6

QD
type: SiteQuality
SIO_000300: 1.188e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 106
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.564296520423601e-4
allele num: 6610
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.715e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

FS
type: SiteQuality
SIO_000300: 1.972e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.45e-1

DP
type: SiteQuality
SIO_000300: 2.725102e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.718e0

MQ
type: SiteQuality
SIO_000300: 5.871e1

QD
type: SiteQuality
SIO_000300: 1.516e1

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817961459217065e-4
allele num: 16502
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 2.158e0

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.725623e6

QD
type: SiteQuality
SIO_000300: 1.13e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.367e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.59e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 96
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variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 2.726298e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.612e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

VQSLOD
type: SiteQuality
SIO_000300: 6.79e-1

QD
type: SiteQuality
SIO_000300: 1.166e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4246
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
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: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.072e-1

QD
type: SiteQuality
SIO_000300: 1.449e1

MQRankSum
type: SiteQuality
SIO_000300: -1.383e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.405e0

DP
type: SiteQuality
SIO_000300: 2.72851e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.992e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 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: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

DP
type: SiteQuality
SIO_000300: 2.729074e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.058e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.002e0

VQSLOD
type: SiteQuality
SIO_000300: 8.38e-1

QD
type: SiteQuality
SIO_000300: 1.196e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.998980173370527e-5
allele num: 66678
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.729587e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.96e-1

FS
type: SiteQuality
SIO_000300: 3.005e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.44e0

QD
type: SiteQuality
SIO_000300: 1.459e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2001
bin: 8.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312673450508788e-4
allele num: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.47e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.729645e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.199999999999999e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 21
bin: 3.25e1
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GenotypeQuality
all individuals: 26115
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2000
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

DP
type: SiteQuality
SIO_000300: 2.72991e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.821e0

FS
type: SiteQuality
SIO_000300: 5.452e0

MQ
type: SiteQuality
SIO_000300: 5.937e1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e-1

QD
type: SiteQuality
SIO_000300: 1.143e1

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

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

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

GenotypeQuality
all individuals: 3848
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5565
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26115
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2602
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3174
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12995
bin: 6.25e1
variant carriers: 0

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: 66684
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 11546
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

QD
type: SiteQuality
SIO_000300: 1.143e1

MQ
type: SiteQuality
SIO_000300: 5.937e1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e-1

FS
type: SiteQuality
SIO_000300: 5.452e0

MQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.821e0

DP
type: SiteQuality
SIO_000300: 2.72991e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

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

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

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

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2602
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13012
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3849
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4246
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
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: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.075e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

QD
type: SiteQuality
SIO_000300: 1.083e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.109e0

VQSLOD
type: SiteQuality
SIO_000300: 8.43e-1

DP
type: SiteQuality
SIO_000300: 2.729889e6

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

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

GenotypeQuality
all individuals: 3850
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2600
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4243
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12972
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999130252226854e-5
allele num: 66686
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 1.49e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

DP
type: SiteQuality
SIO_000300: 2.730195e6

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2595
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5546
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4237
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26100
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
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: 6608
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.066e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

FS
type: SiteQuality
SIO_000300: 3.395e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 2.728425e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4238
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 5550
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2005
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13008
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26103
bin: 9.75e1
variant carriers: 4

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
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: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998410842253606e-5
allele num: 66702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
SIO_000300: 8.98e0

VQSLOD
type: SiteQuality
SIO_000300: 5.649999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.955e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.728282e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3851
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5550
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2597
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3174
bin: 9.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

QD
type: SiteQuality
SIO_000300: 1.055e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.96e-1

DP
type: SiteQuality
SIO_000300: 2.728313e6

GenotypeQuality
all individuals: 2599
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13033
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
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: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497211728728189e-5
allele num: 66708
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.62e-1

DP
type: SiteQuality
SIO_000300: 2.728499e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.216e1

VQSLOD
type: SiteQuality
SIO_000300: 3.97e0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26098
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2599
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4239
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5563
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.096e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 3.106e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e0

FS
type: SiteQuality
SIO_000300: 5.774e0

DP
type: SiteQuality
SIO_000300: 2.728316e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: -2.811e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13065
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3854
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4238
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3174
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2602
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.762e0

MQRankSum
type: SiteQuality
SIO_000300: 9.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.75e-1

DP
type: SiteQuality
SIO_000300: 2.728882e6

QD
type: SiteQuality
SIO_000300: 1.028e1

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26099
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2604
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3856
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5571
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.0122e1

MQRankSum
type: SiteQuality
SIO_000300: 5.47e-1

DP
type: SiteQuality
SIO_000300: 2.728967e6

MQ
type: SiteQuality
SIO_000300: 5.837e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

QD
type: SiteQuality
SIO_000300: 1.399e1

VQSLOD
type: SiteQuality
SIO_000300: -5.098e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3174
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.258e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.702e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 9.096e0

MQRankSum
type: SiteQuality
SIO_000300: 8.22e-1

DP
type: SiteQuality
SIO_000300: 2.728994e6

MQ
type: SiteQuality
SIO_000300: 5.866e1

QD
type: SiteQuality
SIO_000300: 1.091e1

GenotypeQuality
all individuals: 3173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 13081
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26097
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5572
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3854
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
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

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
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: 8652
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 8.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

DP
type: SiteQuality
SIO_000300: 2.729201e6

VQSLOD
type: SiteQuality
SIO_000300: 3.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

QD
type: SiteQuality
SIO_000300: 7.55e0

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

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3854
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 26095
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 5572
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3173
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 2.25e1
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: 8.655011251514626e-5
allele num: 11554
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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 4.51e-1

MQ
type: SiteQuality
SIO_000300: 5.99e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 2.729105e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.301e1

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3854
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13083
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26095
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
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: 11554
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.21e1

VQSLOD
type: SiteQuality
SIO_000300: 7.43e-1

DP
type: SiteQuality
SIO_000300: 2.729095e6

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.11e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 3852
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13088
bin: 6.25e1
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: 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: 66718
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.731301939058172e-4
allele num: 11552
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

QD
type: SiteQuality
SIO_000300: 1.136e1

FS
type: SiteQuality
SIO_000300: 9.319000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.57e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.549e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e-2

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 2.729223e6