10-124358653-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124358653
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124358653
    reference: chr 10
allele count: 7
allele frequency: 5.807779105270144e-5
allele num: 120528
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3280+40A>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3250+40A>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1783+40A>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3250+40A>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-6719A>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1783+40A>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3280+40A>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6255
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3088
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2921
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1556
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

10-124358655-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124358655
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124358655
    reference: chr 10
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1783+42T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3250+42T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-6717T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3280+42T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3280+42T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3250+42T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1783+42T>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5205
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2919
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37504
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-124358661-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124358661
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124358661
    reference: chr 10
allele count: 1
allele frequency: 8.307993951780402e-6
allele num: 120366
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3280+48C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-6711C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3250+48C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1783+48C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3280+48C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1783+48C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3250+48C>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2918
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3088
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2551
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

10-124358662-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124358662
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124358662
    reference: chr 10
allele count: 1
allele frequency: 8.308684236764266e-6
allele num: 120356
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3280+49C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3250+49C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3250+49C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3280+49C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-6710C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1783+49C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1783+49C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6235
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1529
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2810
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37498
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2918
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

10-124359530-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359530
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359530
    reference: chr 10
allele count: 84
allele frequency: 6.986841448605127e-4
allele num: 120226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-50C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5842C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-50C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-50C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-50C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-50C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-50C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52174
  bin: 9.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 5
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

10-124359531-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359531
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359531
    reference: chr 10
allele count: 1
allele frequency: 8.318083513558476e-6
allele num: 120220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-49G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-49G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5841G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-49G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-49G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-49G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-49G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52172
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

10-124359532-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359532
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359532
    reference: chr 10
allele count: 2
allele frequency: 1.663533678239316e-5
allele num: 120226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-48A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-48A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-48A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-48A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-48A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5840A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-48A>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52172
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

10-124359534-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359534
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359534
    reference: chr 10
allele count: 3
allele frequency: 2.495383540450167e-5
allele num: 120222
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-46T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5838T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-46T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-46T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-46T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-46T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-46T>C
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52172
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54669
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

10-124359538-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359538
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359538
    reference: chr 10
allele count: 1
allele frequency: 8.317945134833891e-6
allele num: 120222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-42G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5834G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-42G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-42G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-42G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-42G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-42G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52172
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

10-124359544-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359544
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359544
    reference: chr 10
allele count: 5
allele frequency: 4.158972567416945e-5
allele num: 120222
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-36T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-36T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-36T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5828T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-36T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-36T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-36T>C
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52172
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54668
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-124359545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359545
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359545
    reference: chr 10
allele count: 5
allele frequency: 4.158972567416945e-5
allele num: 120222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-35G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-35G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5827G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-35G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-35G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-35G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-35G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52172
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

10-124359548-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359548
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359548
    reference: chr 10
allele count: 1
allele frequency: 8.318221896887321e-6
allele num: 120218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-32C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-32C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5824C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-32C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-32C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-32C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-32C>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52173
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3024
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

10-124359549-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359549
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359549
    reference: chr 10
allele count: 1
allele frequency: 8.317945134833891e-6
allele num: 120222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-31C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-31C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-31C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-31C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-31C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5823C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-31C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52173
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54668
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

10-124359551-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359551
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359551
    reference: chr 10
allele count: 3
allele frequency: 2.495342028214001e-5
allele num: 120224
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-29G>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-29G>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-29G>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5821G>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-29G>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-29G>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-29G>C
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52173
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54668
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

10-124359558-CCTTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359558
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359553
    reference: chr 10
allele count: 1
allele frequency: 8.317945134833891e-6
allele num: 120222
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-13_1784-9delCTCTT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-13_3251-9delCTCTT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-13_3281-9delCTCTT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5805_671-5801delCTCTT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-13_1784-9delCTCTT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-13_3281-9delCTCTT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-13_3251-9delCTCTT
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52172
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54668
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: CCTTCT
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

10-124359561-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359561
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359561
    reference: chr 10
allele count: 1
allele frequency: 8.31766839119658e-6
allele num: 120226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-19T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-19T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-19T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-19T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-19T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-19T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5811T>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52173
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54669
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3030
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-124359561-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359561
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359558
    reference: chr 10
allele count: 4
allele frequency: 3.327067356478632e-5
allele num: 120226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-18_3281-16delCTC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-18_3281-16delCTC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-18_3251-16delCTC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5810_671-5808delCTC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-18_1784-16delCTC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-18_1784-16delCTC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-18_3251-16delCTC
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52173
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: TCTC
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

10-124359562-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359562
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359562
    reference: chr 10
allele count: 1
allele frequency: 8.317806760713336e-6
allele num: 120224
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-18C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-18C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-18C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5810C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-18C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-18C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-18C>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52170
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54666
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

10-124359564-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359564
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359564
    reference: chr 10
allele count: 6
allele frequency: 4.990850108135085e-5
allele num: 120220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-16C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-16C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-16C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5808C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-16C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-16C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-16C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52174
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54667
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

10-124359574-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359574
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359574
    reference: chr 10
allele count: 2
allele frequency: 1.664004259850905e-5
allele num: 120192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-6T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-6T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5798T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-6T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-6T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-6T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-6T>C
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52172
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: c.3281-6T>C
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-124359575-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359575
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359575
    reference: chr 10
allele count: 2
allele frequency: 1.664031949413429e-5
allele num: 120190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251-5C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281-5C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784-5C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5797C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281-5C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784-5C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251-5C>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52172
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.25e1
  variant carriers: 0
hgvs: c.3281-5C>A
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-124359580-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359580
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359580
    reference: chr 10
allele count: 1
allele frequency: 8.320575118152166e-6
allele num: 120184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784C>A
  hgvsp: ENSP00000327747.4:p.Ala595Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251C>A
  hgvsp: ENSP00000357951.3:p.Ala1084Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251C>A
  hgvsp: ENSP00000343175.3:p.Ala1084Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5792C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784C>A
  hgvsp: ENSP00000357952.2:p.Ala595Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281C>A
  hgvsp: ENSP00000357905.3:p.Ala1094Asp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281C>A
  hgvsp: ENSP00000342210.3:p.Ala1094Asp
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52173
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala1094Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS

10-124359580-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359580
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359580
    reference: chr 10
allele count: 26
allele frequency: 2.163349530719563e-4
allele num: 120184
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3281C>T
  hgvsp: ENSP00000342210.3:p.Ala1094Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3281C>T
  hgvsp: ENSP00000357905.3:p.Ala1094Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3251C>T
  hgvsp: ENSP00000343175.3:p.Ala1084Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3251C>T
  hgvsp: ENSP00000357951.3:p.Ala1084Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1784C>T
  hgvsp: ENSP00000357952.2:p.Ala595Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1784C>T
  hgvsp: ENSP00000327747.4:p.Ala595Val
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5792C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52173
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala1094Val
num of homozygotes: 1
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

10-124359582-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359582
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359582
    reference: chr 10
allele count: 8
allele frequency: 6.657567990413102e-5
allele num: 120164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3283T>C
  hgvsp: ENSP00000342210.3:p.Ser1095Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1786T>C
  hgvsp: ENSP00000357952.2:p.Ser596Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3283T>C
  hgvsp: ENSP00000357905.3:p.Ser1095Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3253T>C
  hgvsp: ENSP00000357951.3:p.Ser1085Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3253T>C
  hgvsp: ENSP00000343175.3:p.Ser1085Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1786T>C
  hgvsp: ENSP00000327747.4:p.Ser596Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5790T>C
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52171
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54663
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser1095Pro
num of homozygotes: 1
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD

10-124359583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359583
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359583
    reference: chr 10
allele count: 1
allele frequency: 8.319467554076538e-6
allele num: 120200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3254C>T
  hgvsp: ENSP00000343175.3:p.Ser1085Phe
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3284C>T
  hgvsp: ENSP00000342210.3:p.Ser1095Phe
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3284C>T
  hgvsp: ENSP00000357905.3:p.Ser1095Phe
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1787C>T
  hgvsp: ENSP00000327747.4:p.Ser596Phe
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1787C>T
  hgvsp: ENSP00000357952.2:p.Ser596Phe
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5789C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3254C>T
  hgvsp: ENSP00000357951.3:p.Ser1085Phe
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52167
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3006
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser1095Phe
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

10-124359585-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359585
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359585
    reference: chr 10
allele count: 1
allele frequency: 8.320436656515735e-6
allele num: 120186
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3256C>G
  hgvsp: ENSP00000357951.3:p.Gln1086Glu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3256C>G
  hgvsp: ENSP00000343175.3:p.Gln1086Glu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1789C>G
  hgvsp: ENSP00000327747.4:p.Gln597Glu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3286C>G
  hgvsp: ENSP00000342210.3:p.Gln1096Glu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3286C>G
  hgvsp: ENSP00000357905.3:p.Gln1096Glu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1789C>G
  hgvsp: ENSP00000357952.2:p.Gln597Glu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5787C>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52167
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln1096Glu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP

10-124359586-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359586
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359586
    reference: chr 10
allele count: 1
allele frequency: 8.320436656515735e-6
allele num: 120186
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3257A>G
  hgvsp: ENSP00000357951.3:p.Gln1086Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1790A>G
  hgvsp: ENSP00000327747.4:p.Gln597Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5786A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3287A>G
  hgvsp: ENSP00000342210.3:p.Gln1096Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3287A>G
  hgvsp: ENSP00000357905.3:p.Gln1096Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1790A>G
  hgvsp: ENSP00000357952.2:p.Gln597Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3257A>G
  hgvsp: ENSP00000343175.3:p.Gln1086Arg
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52167
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2982
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54664
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln1096Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP

10-124359587-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359587
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359587
    reference: chr 10
allele count: 3
allele frequency: 2.49613099695472e-5
allele num: 120186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1791G>T
  hgvsp: ENSP00000327747.4:p.Gln597His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3258G>T
  hgvsp: ENSP00000343175.3:p.Gln1086His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3288G>T
  hgvsp: ENSP00000342210.3:p.Gln1096His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1791G>T
  hgvsp: ENSP00000357952.2:p.Gln597His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5785G>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3258G>T
  hgvsp: ENSP00000357951.3:p.Gln1086His
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3288G>T
  hgvsp: ENSP00000357905.3:p.Gln1096His
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52167
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln1096His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-124359589-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359589
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359589
    reference: chr 10
allele count: 2
allele frequency: 1.664115023630433e-5
allele num: 120184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3290C>A
  hgvsp: ENSP00000342210.3:p.Ser1097Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3260C>A
  hgvsp: ENSP00000357951.3:p.Ser1087Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3290C>A
  hgvsp: ENSP00000357905.3:p.Ser1097Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3260C>A
  hgvsp: ENSP00000343175.3:p.Ser1087Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1793C>A
  hgvsp: ENSP00000357952.2:p.Ser598Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1793C>A
  hgvsp: ENSP00000327747.4:p.Ser598Tyr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5783C>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52167
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2968
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser1097Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

10-124359590-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359590
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359590
    reference: chr 10
allele count: 1
allele frequency: 8.320575118152166e-6
allele num: 120184
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5782C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1794C>T
  hgvsp: ENST00000330163.4:c.1794C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3261C>T
  hgvsp: ENST00000344338.3:c.3261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3291C>T
  hgvsp: ENST00000338354.3:c.3291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3261C>T
  hgvsp: ENST00000368955.3:c.3261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3291C>T
  hgvsp: ENST00000368909.3:c.3291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1794C>T
  hgvsp: ENST00000368956.2:c.1794C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52167
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54665
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser1097Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

10-124359591-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359591
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359591
    reference: chr 10
allele count: 5
allele frequency: 4.160356792198499e-5
allele num: 120182
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3292C>T
  hgvsp: ENSP00000357905.3:p.Arg1098Trp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3262C>T
  hgvsp: ENSP00000343175.3:p.Arg1088Trp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1795C>T
  hgvsp: ENSP00000327747.4:p.Arg599Trp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3262C>T
  hgvsp: ENSP00000357951.3:p.Arg1088Trp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1795C>T
  hgvsp: ENSP00000357952.2:p.Arg599Trp
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5781C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3292C>T
  hgvsp: ENSP00000342210.3:p.Arg1098Trp
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52167
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg1098Trp
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

10-124359592-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359592
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359592
    reference: chr 10
allele count: 139
allele frequency: 1.156636932499001e-3
allele num: 120176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1796G>A
  hgvsp: ENSP00000327747.4:p.Arg599Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3293G>A
  hgvsp: ENSP00000342210.3:p.Arg1098Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3263G>A
  hgvsp: ENSP00000343175.3:p.Arg1088Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3263G>A
  hgvsp: ENSP00000357951.3:p.Arg1088Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5780G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1796G>A
  hgvsp: ENSP00000357952.2:p.Arg599Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3293G>A
  hgvsp: ENSP00000357905.3:p.Arg1098Gln
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52168
  bin: 9.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2973
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg1098Gln
num of homozygotes: 12
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

10-124359592-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359592
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359592
    reference: chr 10
allele count: 1
allele frequency: 8.321129010784183e-6
allele num: 120176
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5780G>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3293G>C
  hgvsp: ENSP00000342210.3:p.Arg1098Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3263G>C
  hgvsp: ENSP00000343175.3:p.Arg1088Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1796G>C
  hgvsp: ENSP00000327747.4:p.Arg599Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3263G>C
  hgvsp: ENSP00000357951.3:p.Arg1088Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1796G>C
  hgvsp: ENSP00000357952.2:p.Arg599Pro
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3293G>C
  hgvsp: ENSP00000357905.3:p.Arg1098Pro
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52168
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg1098Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

10-124359593-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359593
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359593
    reference: chr 10
allele count: 1
allele frequency: 8.321544478655239e-6
allele num: 120170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5779G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3294G>A
  hgvsp: ENST00000368909.3:c.3294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1797G>A
  hgvsp: ENST00000330163.4:c.1797G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1797G>A
  hgvsp: ENST00000368956.2:c.1797G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3264G>A
  hgvsp: ENST00000368955.3:c.3264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3264G>A
  hgvsp: ENST00000344338.3:c.3264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3294G>A
  hgvsp: ENST00000338354.3:c.3294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52161
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2973
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg1098Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD

10-124359593-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359593
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359593
    reference: chr 10
allele count: 44
allele frequency: 3.661479570608305e-4
allele num: 120170
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3264G>C
  hgvsp: ENST00000344338.3:c.3264G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1797G>C
  hgvsp: ENST00000368956.2:c.1797G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1797G>C
  hgvsp: ENST00000330163.4:c.1797G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3264G>C
  hgvsp: ENST00000368955.3:c.3264G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3294G>C
  hgvsp: ENST00000338354.3:c.3294G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5779G>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3294G>C
  hgvsp: ENST00000368909.3:c.3294G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52161
  bin: 9.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54652
  bin: 9.75e1
  variant carriers: 40
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg1098Arg
num of homozygotes: 3
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/10-124359595-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359595
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359595
    reference: chr 10
allele count: 1
allele frequency: 8.321405984755183e-6
allele num: 120172
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3296C>A
  hgvsp: ENSP00000357905.3:p.Pro1099Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1799C>A
  hgvsp: ENSP00000327747.4:p.Pro600Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3296C>A
  hgvsp: ENSP00000342210.3:p.Pro1099Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3266C>A
  hgvsp: ENSP00000343175.3:p.Pro1089Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1799C>A
  hgvsp: ENSP00000357952.2:p.Pro600Gln
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5777C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3266C>A
  hgvsp: ENSP00000357951.3:p.Pro1089Gln
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52159
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54648
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro1099Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

10-124359596-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359596
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359596
    reference: chr 10
allele count: 13
allele frequency: 1.082070917263193e-4
allele num: 120140
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1800A>G
  hgvsp: ENST00000368956.2:c.1800A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3297A>G
  hgvsp: ENST00000338354.3:c.3297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3267A>G
  hgvsp: ENST00000344338.3:c.3267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3267A>G
  hgvsp: ENST00000368955.3:c.3267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3297A>G
  hgvsp: ENST00000368909.3:c.3297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5776A>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1800A>G
  hgvsp: ENST00000330163.4:c.1800A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52159
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54651
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2967
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.25e1
  variant carriers: 1
hgvs: p.Pro1099Pro
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/10-124359600-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359600
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359600
    reference: chr 10
allele count: 1
allele frequency: 8.32279113123377e-6
allele num: 120152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3301C>A
  hgvsp: ENSP00000342210.3:p.Pro1101Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1804C>A
  hgvsp: ENSP00000327747.4:p.Pro602Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3271C>A
  hgvsp: ENSP00000357951.3:p.Pro1091Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3301C>A
  hgvsp: ENSP00000357905.3:p.Pro1101Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5772C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1804C>A
  hgvsp: ENSP00000357952.2:p.Pro602Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3271C>A
  hgvsp: ENSP00000343175.3:p.Pro1091Thr
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52159
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro1101Thr
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ

10-124359600-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359600
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359600
    reference: chr 10
allele count: 5
allele frequency: 4.161395565616885e-5
allele num: 120152
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1804C>G
  hgvsp: ENSP00000327747.4:p.Pro602Ala
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3301C>G
  hgvsp: ENSP00000357905.3:p.Pro1101Ala
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3271C>G
  hgvsp: ENSP00000343175.3:p.Pro1091Ala
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1804C>G
  hgvsp: ENSP00000357952.2:p.Pro602Ala
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3301C>G
  hgvsp: ENSP00000342210.3:p.Pro1101Ala
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5772C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3271C>G
  hgvsp: ENSP00000357951.3:p.Pro1091Ala
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52159
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro1101Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

10-124359601-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359601
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359601
    reference: chr 10
allele count: 8
allele frequency: 6.658454572693678e-5
allele num: 120148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5771C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1805C>G
  hgvsp: ENSP00000357952.2:p.Pro602Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1805C>G
  hgvsp: ENSP00000327747.4:p.Pro602Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3272C>G
  hgvsp: ENSP00000357951.3:p.Pro1091Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3272C>G
  hgvsp: ENSP00000343175.3:p.Pro1091Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3302C>G
  hgvsp: ENSP00000357905.3:p.Pro1101Arg
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3302C>G
  hgvsp: ENSP00000342210.3:p.Pro1101Arg
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52159
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54645
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro1101Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

10-124359602-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359602
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359602
    reference: chr 10
allele count: 18
allele frequency: 1.498401704848162e-4
allele num: 120128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5770T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1806T>C
  hgvsp: ENST00000368956.2:c.1806T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3303T>C
  hgvsp: ENST00000368909.3:c.3303T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3273T>C
  hgvsp: ENST00000368955.3:c.3273T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3273T>C
  hgvsp: ENST00000344338.3:c.3273T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1806T>C
  hgvsp: ENST00000330163.4:c.1806T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3303T>C
  hgvsp: ENST00000338354.3:c.3303T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52159
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 2
hgvs: p.Pro1101Pro
num of homozygotes: 2
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-124359604-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359604
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359604
    reference: chr 10
allele count: 3
allele frequency: 2.497793615639518e-5
allele num: 120106
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1808G>C
  hgvsp: ENSP00000327747.4:p.Ser603Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3305G>C
  hgvsp: ENSP00000342210.3:p.Ser1102Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1808G>C
  hgvsp: ENSP00000357952.2:p.Ser603Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5768G>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3275G>C
  hgvsp: ENSP00000357951.3:p.Ser1092Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3275G>C
  hgvsp: ENSP00000343175.3:p.Ser1092Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3305G>C
  hgvsp: ENSP00000357905.3:p.Ser1102Thr
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 2
hgvs: p.Ser1102Thr
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

10-124359605-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359605
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359605
    reference: chr 10
allele count: 8
allele frequency: 6.661004812575977e-5
allele num: 120102
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3276T>C
  hgvsp: ENST00000344338.3:c.3276T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3306T>C
  hgvsp: ENST00000338354.3:c.3306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5767T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1809T>C
  hgvsp: ENST00000330163.4:c.1809T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3306T>C
  hgvsp: ENST00000368909.3:c.3306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3276T>C
  hgvsp: ENST00000368955.3:c.3276T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1809T>C
  hgvsp: ENST00000368956.2:c.1809T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52158
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2851
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser1102Ser
num of homozygotes: 1
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/10-124359606-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359606
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359606
    reference: chr 10
allele count: 1
allele frequency: 8.324315325064513e-6
allele num: 120130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3277C>A
  hgvsp: ENSP00000357951.3:p.Pro1093Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3307C>A
  hgvsp: ENSP00000357905.3:p.Pro1103Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1810C>A
  hgvsp: ENSP00000327747.4:p.Pro604Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1810C>A
  hgvsp: ENSP00000357952.2:p.Pro604Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3277C>A
  hgvsp: ENSP00000343175.3:p.Pro1093Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3307C>A
  hgvsp: ENSP00000342210.3:p.Pro1103Thr
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5766C>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52157
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro1103Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD

10-124359607-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359607
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359607
    reference: chr 10
allele count: 1
allele frequency: 8.324176738920521e-6
allele num: 120132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3308C>T
  hgvsp: ENSP00000342210.3:p.Pro1103Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5765C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3278C>T
  hgvsp: ENSP00000343175.3:p.Pro1093Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3308C>T
  hgvsp: ENSP00000357905.3:p.Pro1103Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1811C>T
  hgvsp: ENSP00000357952.2:p.Pro604Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3278C>T
  hgvsp: ENSP00000357951.3:p.Pro1093Leu
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1811C>T
  hgvsp: ENSP00000327747.4:p.Pro604Leu
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52157
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2885
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro1103Leu
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

10-124359611-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359611
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359611
    reference: chr 10
allele count: 1
allele frequency: 8.324869715788949e-6
allele num: 120122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+2T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+2T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+2T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+2T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+2T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+2T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5761T>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52157
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: c.3310+2T>G
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

10-124359612-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359612
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359612
    reference: chr 10
allele count: 14
allele frequency: 1.16649169291273e-4
allele num: 120018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+3G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+3G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5760G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+3G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+3G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+3G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+3G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52157
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 54646
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
hgvs: c.3310+3G>A
num of homozygotes: 1
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

10-124359613-GGTCCCCAGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359613
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359604
    reference: chr 10
allele count: 1
allele frequency: 8.323622440486099e-6
allele num: 120140
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52157
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
hgvs: c.3310+9_3310+17delCCAGTGTCC
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: GGTCCCCAGT
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

10-124359615-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359615
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359615
    reference: chr 10
allele count: 2
allele frequency: 1.664835347784104e-5
allele num: 120132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+6T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+6T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+6T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5757T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+6T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+6T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+6T>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52157
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54644
  bin: 9.75e1
  variant carriers: 2
hgvs: c.3310+6T>A
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

10-124359615-T-TCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359615
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359618
    reference: chr 10
allele count: 1
allele frequency: 8.324176738920521e-6
allele num: 120132
alternate allele: TCCC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+8_3310+10dupCCC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+8_3310+10dupCCC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+8_1813+10dupCCC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+8_3280+10dupCCC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+8_3280+10dupCCC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+8_1813+10dupCCC
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5755_671-5753dupCCC
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52157
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2770
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
hgvs: c.3310+8_3310+10dupCCC
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/10-124359616-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359616
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359616
    reference: chr 10
allele count: 1
allele frequency: 8.324592511196577e-6
allele num: 120126
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+7C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5756C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+7C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+7C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+7C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+7C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+7C>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52156
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
hgvs: c.3310+7C>A
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

10-124359616-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359616
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359616
    reference: chr 10
allele count: 1
allele frequency: 8.324592511196577e-6
allele num: 120126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+7C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+7C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+7C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+7C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+7C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5756C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+7C>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52156
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2779
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
hgvs: c.3310+7C>G
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

10-124359617-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359617
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359617
    reference: chr 10
allele count: 1
allele frequency: 8.324731111185109e-6
allele num: 120124
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5755C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+8C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+8C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+8C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+8C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+8C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+8C>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52157
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54643
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
hgvs: c.3310+8C>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

10-124359617-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359617
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359617
    reference: chr 10
allele count: 14
allele frequency: 1.165462355565915e-4
allele num: 120124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+8C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+8C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5755C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+8C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+8C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+8C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+8C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52157
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
hgvs: c.3310+8C>T
num of homozygotes: 3
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

10-124359619-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359619
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359619
    reference: chr 10
allele count: 2
allele frequency: 1.665057111458923e-5
allele num: 120116
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+10C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5753C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+10C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+10C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+10C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+10C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+10C>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54641
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS

10-124359624-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359624
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359624
    reference: chr 10
allele count: 1
allele frequency: 8.327920185212944e-6
allele num: 120078
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5748T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+15T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+15T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+15T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+15T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+15T>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+15T>C
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

10-124359625-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359625
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359625
    reference: chr 10
allele count: 1
allele frequency: 8.328613785521537e-6
allele num: 120068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5747C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+16C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+16C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+16C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+16C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+16C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+16C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54641
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

10-124359626-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359626
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359626
    reference: chr 10
allele count: 1
allele frequency: 8.330001332800213e-6
allele num: 120048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+17C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+17C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5746C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+17C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+17C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+17C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+17C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52155
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54640
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

10-124359628-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359628
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359628
    reference: chr 10
allele count: 1
allele frequency: 8.329723786359244e-6
allele num: 120052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+19T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+19T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+19T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+19T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5744T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+19T>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+19T>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/10-124359634-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359634
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359634
    reference: chr 10
allele count: 113
allele frequency: 9.429081624138449e-4
allele num: 119842
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5738A>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+25A>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+25A>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+25A>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+25A>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+25A>C
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+25A>C
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 52173
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 2.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 6.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 7.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 54639
  bin: 9.75e1
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.5e0
  variant carriers: 3
num of homozygotes: 9
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

10-124359638-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359638
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359638
    reference: chr 10
allele count: 1
allele frequency: 8.328891257995735e-6
allele num: 120064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5734G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+29G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+29G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+29G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+29G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+29G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+29G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52161
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

10-124359639-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359639
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359639
    reference: chr 10
allele count: 1
allele frequency: 8.329030001166064e-6
allele num: 120062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+30T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5733T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+30T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+30T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+30T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+30T>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+30T>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52161
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-124359640-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359640
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359640
    reference: chr 10
allele count: 380
allele frequency: 3.165347771761766e-3
allele num: 120050
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+31C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+31C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+31C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5732C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+31C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+31C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+31C>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52164
  bin: 9.75e1
  variant carriers: 324
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 36
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum

10-124359640-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359640
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359640
    reference: chr 10
allele count: 1
allele frequency: 8.329862557267805e-6
allele num: 120050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+31C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+31C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+31C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5732C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+31C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+31C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+31C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52164
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

10-124359641-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359641
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359641
    reference: chr 10
allele count: 3
allele frequency: 2.499083669321249e-5
allele num: 120044
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+32C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5731C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+32C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+32C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+32C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+32C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+32C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52145
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54622
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

10-124359647-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359647
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359647
    reference: chr 10
allele count: 1
allele frequency: 8.331250520703158e-6
allele num: 120030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+38C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+38C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+38C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5725C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+38C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+38C>T
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+38C>T
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52145
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-124359654-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124359654
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124359654
    reference: chr 10
allele count: 21
allele frequency: 1.752511933771739e-4
allele num: 119828
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-5718C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3280+45C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3310+45C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3280+45C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1813+45C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1813+45C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3310+45C>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52145
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54626
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/10-124360483-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124360483
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124360483
    reference: chr 10
allele count: 1
allele frequency: 6.490134994807892e-5
allele num: 15408
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3311-24C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-4889C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1814-24C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3281-24C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1814-24C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3281-24C>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3311-24C>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25573
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24177
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-124360483-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124360483
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124360483
    reference: chr 10
allele count: 1
allele frequency: 6.490134994807892e-5
allele num: 15408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-4889C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3281-24C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3311-24C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1814-24C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1814-24C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3311-24C>G
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3281-24C>G
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24177
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25573
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

10-124360489-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124360489
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124360490
    reference: chr 10
allele count: 21
allele frequency: 1.221072217699733e-3
allele num: 17198
alternate allele: CT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3311-15dupT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-4880dupT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1814-15dupT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3281-15dupT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3281-15dupT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1814-15dupT
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3311-15dupT
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31363
  bin: 7.5e0
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18604
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18264
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

10-124360493-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124360493
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124360493
    reference: chr 10
allele count: 1
allele frequency: 5.217028380634391e-5
allele num: 19168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3311-14G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3281-14G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-4879G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3311-14G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1814-14G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3281-14G>A
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1814-14G>A
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34281
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15047
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3809
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34595
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14820
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

10-124360498-AATTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124360498
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 124360494
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 21872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357951
  ensembl transcript: ENST00000368955
  gene symbol: DMBT1
  hgvsc: ENST00000368955.3:c.3281-7_3281-4delTTTA
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000352593
  ensembl transcript: ENST00000359586
  gene symbol: DMBT1
  hgvsc: ENST00000359586.6:c.671-4872_671-4869delTTTA
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000342210
  ensembl transcript: ENST00000338354
  gene symbol: DMBT1
  hgvsc: ENST00000338354.3:c.3311-7_3311-4delTTTA
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000343175
  ensembl transcript: ENST00000344338
  gene symbol: DMBT1
  hgvsc: ENST00000344338.3:c.3281-7_3281-4delTTTA
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357952
  ensembl transcript: ENST00000368956
  gene symbol: DMBT1
  hgvsc: ENST00000368956.2:c.1814-7_1814-4delTTTA
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000357905
  ensembl transcript: ENST00000368909
  gene symbol: DMBT1
  hgvsc: ENST00000368909.3:c.3311-7_3311-4delTTTA
  variant of: http://identifiers.org/hgnc/2926
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000187908
  ensembl protein: ENSP00000327747
  ensembl transcript: ENST00000330163
  gene symbol: DMBT1
  hgvsc: ENST00000330163.4:c.1814-7_1814-4delTTTA
  variant of: http://identifiers.org/hgnc/2926
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35981
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
hgvs: c.3311-7_3311-4delTTTA
num of homozygotes: 0
reference allele: AATTT

GenotypeQuality
all individuals: 586
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1658
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5022
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37506
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 402
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2810
bin: 6.75e1
variant carriers: 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: 8610
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
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: 3
allele frequency: 4.503828254015913e-5
allele num: 66610
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.423948612289419e-4
allele num: 16502
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 5.813e0

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

MQ
type: SiteQuality
SIO_000300: 5.409e1

DP
type: SiteQuality
SIO_000300: 3.103442e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.112e0

QD
type: SiteQuality
SIO_000300: 1.34e1

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 302
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2828
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1657
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3090
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
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: 896
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.644e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.102964e6

QD
type: SiteQuality
SIO_000300: 9.73e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

MQRankSum
type: SiteQuality
SIO_000300: -1.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.273e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

GenotypeQuality
all individuals: 701
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2808
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37499
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3237
bin: 6.25e1
variant carriers: 0

South Asian
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allele frequency: 6.065752759917505e-5
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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SIO_000300: 2.22e0

ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
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MQRankSum
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VQSLOD
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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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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66520
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 11558
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South Asian
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allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

DP
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FS
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
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MQRankSum
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QD
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MQ
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SIO_000300: 5.608e1

ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 75

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 5.06591796875e-3
allele num: 16384
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Latino
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European (Non-Finnish)
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allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

African
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East Asian
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Other
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BaseQRankSum
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SIO_000300: 1.62e0

InbreedingCoeff
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ClippingRankSum
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FS
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MQ
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SIO_000300: 5.621e1

MQRankSum
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VQSLOD
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SIO_000300: -4.407e-1

ReadPosRankSum
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DP
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SIO_000300: 1.130644e7

QD
type: SiteQuality
SIO_000300: 1.593e1

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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South Asian
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
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Latino
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allele frequency: 8.787346221441125e-5
allele num: 11380
num of homozygotes: 0

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

MQ
type: SiteQuality
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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DP
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FS
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

East Asian
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allele num: 8566
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South Asian
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allele frequency: 0.0e0
allele num: 16386
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9704
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.0051e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.24e-1

MQ
type: SiteQuality
SIO_000300: 5.492e1

BaseQRankSum
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SIO_000300: 9.52e0

InbreedingCoeff
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SIO_000300: 1.9e-3

DP
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SIO_000300: 1.1304816e7

VQSLOD
type: SiteQuality
SIO_000300: -2.061e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16384
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.498695378340282e-5
allele num: 66686
num of homozygotes: 0

East Asian
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num of homozygotes: 0

African
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Other
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ReadPosRankSum
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SIO_000300: 1.49e-1

VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.31e-2

FS
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MQ
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MQRankSum
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 16384
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Latino
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African
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allele frequency: 0.0e0
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East Asian
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num of homozygotes: 0

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

Other
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allele num: 894
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 66686
num of homozygotes: 0

African
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Other
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FS
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DP
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MQ
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InbreedingCoeff
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QD
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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East Asian
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Latino
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African
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South Asian
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European (Non-Finnish)
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allele num: 66686
num of homozygotes: 0

ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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FS
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QD
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MQ
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3023
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 1.497e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

InbreedingCoeff
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SIO_000300: 3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.387e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

DP
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SIO_000300: 1.130474e7

ClippingRankSum
type: SiteQuality
SIO_000300: 4.83e-1

MQ
type: SiteQuality
SIO_000300: 5.768e1

QD
type: SiteQuality
SIO_000300: 1.371e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.334812047630166e-4
allele num: 8566
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.104260774020266e-5
allele num: 16382
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.99e-1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 9.723000000000001e0

QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -4.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -1.596e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.531e1

DP
type: SiteQuality
SIO_000300: 1.1304968e7

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

QD
type: SiteQuality
SIO_000300: 1.015e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.45e-1

FS
type: SiteQuality
SIO_000300: 1.0627e1

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.573e1

DP
type: SiteQuality
SIO_000300: 1.1304697e7

VQSLOD
type: SiteQuality
SIO_000300: -4.119e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16382
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
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allele count: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

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

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

VQSLOD
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SIO_000300: 2.7e0

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.28e-1

BaseQRankSum
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DP
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SIO_000300: 1.1304851e7

InbreedingCoeff
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SIO_000300: 2.28e-2

QD
type: SiteQuality
SIO_000300: 1.356e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.24e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11390
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
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allele count: 4
allele frequency: 4.122861265718408e-4
allele num: 9702
num of homozygotes: 1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.1304851e7

MQRankSum
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.602e1

InbreedingCoeff
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SIO_000300: 2.28e-2

BaseQRankSum
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SIO_000300: -1.517e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

FS
type: SiteQuality
SIO_000300: 5.28e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

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

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

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

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

East Asian
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allele frequency: 1.167133520074697e-4
allele num: 8568
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.123e0

MQRankSum
type: SiteQuality
SIO_000300: 9.49e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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MQ
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SIO_000300: 5.538e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.37e-1

DP
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
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allele frequency: 5.267778753292362e-4
allele num: 11390
num of homozygotes: 1

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

MQ
type: SiteQuality
SIO_000300: 5.591e1

FS
type: SiteQuality
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VQSLOD
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 1.18e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.565e1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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QD
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ClippingRankSum
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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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variant carriers: 0

South Asian
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allele count: 0
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allele num: 16368
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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QD
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VQSLOD
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.1306739e7

MQRankSum
type: SiteQuality
SIO_000300: 4.81e-1

QD
type: SiteQuality
SIO_000300: 1.136e1

VQSLOD
type: SiteQuality
SIO_000300: 7.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.344e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.080000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.549e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.02e-2

FS
type: SiteQuality
SIO_000300: 5.34e-1

GenotypeQuality
all individuals: 3007
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54668
bin: 9.75e1
variant carriers: 25

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

East Asian
type: Population
allele count: 11
allele frequency: 1.284146626196591e-3
allele num: 8566
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.113216774666829e-5
allele num: 16358
num of homozygotes: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.391357807834182e-4
allele num: 11386
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 5.161023947151115e-4
allele num: 9688
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.998440405494571e-5
allele num: 66684
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 1.136e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.344e0

VQSLOD
type: SiteQuality
SIO_000300: 7.99e-1

MQ
type: SiteQuality
SIO_000300: 5.549e1

MQRankSum
type: SiteQuality
SIO_000300: 4.81e-1

DP
type: SiteQuality
SIO_000300: 1.1306739e7

FS
type: SiteQuality
SIO_000300: 5.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.080000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.02e-2

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
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variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3005
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variant carriers: 1

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.787346221441125e-5
allele num: 11380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.065688907250568e-4
allele num: 9682
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.99880023995201e-5
allele num: 66680
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.114711997064938e-5
allele num: 16354
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.424e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 3.915e1

MQRankSum
type: SiteQuality
SIO_000300: -2.219e0

DP
type: SiteQuality
SIO_000300: 1.130397e7

FS
type: SiteQuality
SIO_000300: 5.291e0

QD
type: SiteQuality
SIO_000300: 9.69e0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 289
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54664
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.1e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.69e-1

FS
type: SiteQuality
SIO_000300: 4.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

DP
type: SiteQuality
SIO_000300: 1.1302888e7

BaseQRankSum
type: SiteQuality
SIO_000300: -2.527e0

VQSLOD
type: SiteQuality
SIO_000300: -9.185e-1

MQ
type: SiteQuality
SIO_000300: 5.531e1

GenotypeQuality
all individuals: 124
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54664
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 289
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variant carriers: 0

GenotypeQuality
all individuals: 2971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.882e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.443e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.1e0

MQ
type: SiteQuality
SIO_000300: 5.585e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.632e0

DP
type: SiteQuality
SIO_000300: 1.1302489e7

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 358
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variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.770391159445712e-5
allele num: 11402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.633e0

MQ
type: SiteQuality
SIO_000300: 5.583e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

QD
type: SiteQuality
SIO_000300: 1.155e1

VQSLOD
type: SiteQuality
SIO_000300: -1.594e0

FS
type: SiteQuality
SIO_000300: 3.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.38e0

DP
type: SiteQuality
SIO_000300: 1.1302453e7

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

GenotypeQuality
all individuals: 104
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2988
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 404
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variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54665
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 288
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.031991744066047e-4
allele num: 9690
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.334812047630166e-4
allele num: 8566
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.62e-1

FS
type: SiteQuality
SIO_000300: 1.778e0

MQ
type: SiteQuality
SIO_000300: 5.575e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.081e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.21e0

DP
type: SiteQuality
SIO_000300: 1.1302702e7

QD
type: SiteQuality
SIO_000300: 1.035e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 54665
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 999
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
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: 8566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999490086685263e-5
allele num: 66678
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.187e0

QD
type: SiteQuality
SIO_000300: 1.147e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

VQSLOD
type: SiteQuality
SIO_000300: -1.767e0

MQ
type: SiteQuality
SIO_000300: 5.554e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

DP
type: SiteQuality
SIO_000300: 1.1302289e7

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

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

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

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 153
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2958
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.254e1

MQ
type: SiteQuality
SIO_000300: 5.521e1

FS
type: SiteQuality
SIO_000300: 5.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.235e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.1302044e7

VQSLOD
type: SiteQuality
SIO_000300: -9.778e-1

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54665
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2966
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.119202056051891e-5
allele num: 16342
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.032204789430223e-4
allele num: 9688
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.75377060680463e-4
allele num: 11404
num of homozygotes: 1

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

FS
type: SiteQuality
SIO_000300: 5.984e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.84e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.104e-1

DP
type: SiteQuality
SIO_000300: 1.1302333e7

BaseQRankSum
type: SiteQuality
SIO_000300: 7.03e-1

MQ
type: SiteQuality
SIO_000300: 5.684e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.32e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.53e-1

QD
type: SiteQuality
SIO_000300: 1.673e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

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

GenotypeQuality
all individuals: 403
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 54663
bin: 9.75e1
variant carriers: 127

GenotypeQuality
all individuals: 993
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 354
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 106
allele frequency: 1.09391124871001e-2
allele num: 9690
num of homozygotes: 10

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.199832023516708e-4
allele num: 66676
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.630655910206945e-4
allele num: 11404
num of homozygotes: 1

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

South Asian
type: Population
allele count: 22
allele frequency: 1.346718903036239e-3
allele num: 16336
num of homozygotes: 1

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

DP
type: SiteQuality
SIO_000300: 1.1316677e7

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

MQ
type: SiteQuality
SIO_000300: 5.621e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.023e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

QD
type: SiteQuality
SIO_000300: 1.504e1

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

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

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 354
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54663
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2973
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
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: 16336
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

QD
type: SiteQuality
SIO_000300: 1.504e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQ
type: SiteQuality
SIO_000300: 5.621e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.023e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

DP
type: SiteQuality
SIO_000300: 1.1316677e7

GenotypeQuality
all individuals: 285
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 54652
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9688
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.06e-2

DP
type: SiteQuality
SIO_000300: 1.1303992e7

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 5.635e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.349e1

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2973
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 285
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 28
allele frequency: 4.199412082308477e-4
allele num: 66676
num of homozygotes: 2

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.096614368290669e-4
allele num: 9688
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.768853034023149e-5
allele num: 11404
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 6.734419003305988e-4
allele num: 16334
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 1.1303992e7

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 5.635e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.06e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

QD
type: SiteQuality
SIO_000300: 1.349e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.08e-1

GenotypeQuality
all individuals: 148
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 402
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 6.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQ
type: SiteQuality
SIO_000300: 5.624e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.984e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.298e0

FS
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 1.1298233e7

QD
type: SiteQuality
SIO_000300: 1.117e1

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 89
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 400
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.12369871402327e-5
allele num: 16330
num of homozygotes: 0

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

African
type: Population
allele count: 8
allele frequency: 8.261049153242462e-4
allele num: 9684
num of homozygotes: 1

Latino
type: Population
allele count: 3
allele frequency: 2.633889376646181e-4
allele num: 11390
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.1456e1

MQRankSum
type: SiteQuality
SIO_000300: -5.658e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

MQ
type: SiteQuality
SIO_000300: 5.001e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.32e-2

QD
type: SiteQuality
SIO_000300: 1.181e1

VQSLOD
type: SiteQuality
SIO_000300: -3.066e0

DP
type: SiteQuality
SIO_000300: 1.129801e7

GenotypeQuality
all individuals: 986
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2942
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54646
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 397
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 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: 66666
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.127450980392157e-5
allele num: 16320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.48e-1

FS
type: SiteQuality
SIO_000300: 1.106e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.244e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.49e0

DP
type: SiteQuality
SIO_000300: 1.1297921e7

QD
type: SiteQuality
SIO_000300: 1.444e1

MQ
type: SiteQuality
SIO_000300: 5.677e1

GenotypeQuality
all individuals: 54646
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2942
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 986
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.500075000750007e-5
allele num: 66666
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.677e1

VQSLOD
type: SiteQuality
SIO_000300: -9.244e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.67e-1

DP
type: SiteQuality
SIO_000300: 1.1297921e7

BaseQRankSum
type: SiteQuality
SIO_000300: 3.49e0

FS
type: SiteQuality
SIO_000300: 1.106e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.444e1

GenotypeQuality
all individuals: 171
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2932
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 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: 7
allele frequency: 1.050042001680067e-4
allele num: 66664
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.770391159445712e-5
allele num: 11402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 5.644e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.038e0

DP
type: SiteQuality
SIO_000300: 1.1298194e7

BaseQRankSum
type: SiteQuality
SIO_000300: -4.914e0

QD
type: SiteQuality
SIO_000300: 1.266e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.96e-1

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2932
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 348
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54648
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.000060000600006e-5
allele num: 66666
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.633426966292135e-4
allele num: 11392
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.838685952439323e-4
allele num: 16316
num of homozygotes: 1

African
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allele count: 8
allele frequency: 8.259343382201115e-4
allele num: 9686
num of homozygotes: 1

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

FS
type: SiteQuality
SIO_000300: 7.346e0

DP
type: SiteQuality
SIO_000300: 1.1297346e7

MQ
type: SiteQuality
SIO_000300: 4.993e1

BaseQRankSum
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QD
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SIO_000300: 1.595e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.77e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.541e0

VQSLOD
type: SiteQuality
SIO_000300: -2.084e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.756543123133673e-4
allele num: 11386
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.72e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQ
type: SiteQuality
SIO_000300: 3.444e1

MQRankSum
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DP
type: SiteQuality
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QD
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FS
type: SiteQuality
SIO_000300: 8.096e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.867e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500315022051544e-5
allele num: 66662
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.756234632946962e-4
allele num: 11388
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.840716652349982e-4
allele num: 16298
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.87e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.1295539e7

MQ
type: SiteQuality
SIO_000300: 5.026e1

MQRankSum
type: SiteQuality
SIO_000300: -2.183e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

QD
type: SiteQuality
SIO_000300: 2.436e1

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
all individuals: 152
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11412
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: 16298
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.129522e7

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.442e0

MQRankSum
type: SiteQuality
SIO_000300: 4.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.582e0

MQ
type: SiteQuality
SIO_000300: 5.711e1

FS
type: SiteQuality
SIO_000300: 1.779e0

QD
type: SiteQuality
SIO_000300: 1.005e1

GenotypeQuality
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bin: 6.75e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 389
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GenotypeQuality
all individuals: 13
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variant carriers: 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: 8566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

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

European (Finnish)
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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: 16302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.1295151e7

FS
type: SiteQuality
SIO_000300: 4.107e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.12e-1

MQ
type: SiteQuality
SIO_000300: 5.675e1

MQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.946e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.498e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.128e0

QD
type: SiteQuality
SIO_000300: 1.101e1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.137228427642077e-5
allele num: 16294
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9690
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.72e0

FS
type: SiteQuality
SIO_000300: 7.085e0

QD
type: SiteQuality
SIO_000300: 1.226e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.63e-1

MQ
type: SiteQuality
SIO_000300: 5.584e1

VQSLOD
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
SIO_000300: 1.1294555e7

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
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Latino
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allele frequency: 5.275189027606822e-4
allele num: 11374
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South Asian
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allele count: 1
allele frequency: 6.150818058801821e-5
allele num: 16258
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African
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allele frequency: 0.0e0
allele num: 9682
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European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.003331232556046e-5
allele num: 66642
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

MQ
type: SiteQuality
SIO_000300: 5.24e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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MQRankSum
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SIO_000300: -1.67e0

FS
type: SiteQuality
SIO_000300: 5.48e-1

DP
type: SiteQuality
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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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variant carriers: 0

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

Other
type: Population
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allele num: 896
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Latino
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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
allele num: 9692
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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South Asian
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allele frequency: 6.142506142506142e-5
allele num: 16280
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.043e0

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

QD
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MQ
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.1293524e7

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

Latino
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allele num: 11426
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South Asian
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allele num: 16280
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
type: Population
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.59e1

VQSLOD
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QD
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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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Other
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allele num: 894
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 9690
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66662
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South Asian
type: Population
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Latino
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allele count: 1
allele frequency: 8.751969193068441e-5
allele num: 11426
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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QD
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FS
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ClippingRankSum
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VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: -7.28e-1

MQ
type: SiteQuality
SIO_000300: 5.59e1

DP
type: SiteQuality
SIO_000300: 1.1292916e7

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2779
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54643
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.032204789430223e-4
allele num: 9688
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.218e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.124e0

FS
type: SiteQuality
SIO_000300: 4.414e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 5.589e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.337e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 1.129288e7

QD
type: SiteQuality
SIO_000300: 1.23e1

GenotypeQuality
all individuals: 275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54643
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 915
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.032204789430223e-4
allele num: 9688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 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: 66656
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.124e0

VQSLOD
type: SiteQuality
SIO_000300: -1.218e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.23e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.337e0

DP
type: SiteQuality
SIO_000300: 1.129288e7

MQ
type: SiteQuality
SIO_000300: 5.589e1

FS
type: SiteQuality
SIO_000300: 4.414e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2798
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.803e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-2

FS
type: SiteQuality
SIO_000300: 5.56e-1

QD
type: SiteQuality
SIO_000300: 1.433e1

DP
type: SiteQuality
SIO_000300: 1.1293832e7

ClippingRankSum
type: SiteQuality
SIO_000300: -1.68e-1

MQ
type: SiteQuality
SIO_000300: 5.55e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e-1

GenotypeQuality
all individuals: 275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2798
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54643
bin: 9.75e1
variant carriers: 11

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 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: 66656
num of homozygotes: 0

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

Latino
type: Population
allele count: 14
allele frequency: 1.225061253062653e-3
allele num: 11428
num of homozygotes: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.433e1

FS
type: SiteQuality
SIO_000300: 5.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.803e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e-1

DP
type: SiteQuality
SIO_000300: 1.1293832e7

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.55e1

GenotypeQuality
all individuals: 2724
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.22955858846674e-4
allele num: 16266
num of homozygotes: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.1e-1

QD
type: SiteQuality
SIO_000300: 3.145e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.88e-2

MQ
type: SiteQuality
SIO_000300: 5.678e1

DP
type: SiteQuality
SIO_000300: 1.1291649e7

VQSLOD
type: SiteQuality
SIO_000300: -1.388e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.8e-2

FS
type: SiteQuality
SIO_000300: 2.184e0

GenotypeQuality
all individuals: 125
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2628
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54641
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 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: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16234
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

QD
type: SiteQuality
SIO_000300: 1.405e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

FS
type: SiteQuality
SIO_000300: 1.045e0

VQSLOD
type: SiteQuality
SIO_000300: -1.571e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 5.421e1

DP
type: SiteQuality
SIO_000300: 1.1289966e7

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.48e-1

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.0315659170621e-4
allele num: 9694
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 8.43e-1

FS
type: SiteQuality
SIO_000300: 1.082e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e-1

MQ
type: SiteQuality
SIO_000300: 5.544e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.351000000000001e0

DP
type: SiteQuality
SIO_000300: 1.1289439e7

VQSLOD
type: SiteQuality
SIO_000300: -9.432e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 147
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2595
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
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: 16216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

VQSLOD
type: SiteQuality
SIO_000300: -2.199e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.708e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

FS
type: SiteQuality
SIO_000300: 1.0684e1

DP
type: SiteQuality
SIO_000300: 1.1288926e7

MQ
type: SiteQuality
SIO_000300: 5.522e1

QD
type: SiteQuality
SIO_000300: 1.143e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.31e-1

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2557
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54640
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 147
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.750437521876094e-5
allele num: 11428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.59e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.237e0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.43e0

FS
type: SiteQuality
SIO_000300: 1.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.61e-1

DP
type: SiteQuality
SIO_000300: 1.1287923e7

MQ
type: SiteQuality
SIO_000300: 5.376e1

QD
type: SiteQuality
SIO_000300: 1.353e1

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 10

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 200
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 293
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 266
bin: 8.25e1
variant carriers: 8

GenotypeQuality
all individuals: 93
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 9.25e1
variant carriers: 6

Latino
type: Population
allele count: 51
allele frequency: 4.455705049799056e-3
allele num: 11446
num of homozygotes: 2

East Asian
type: Population
allele count: 11
allele frequency: 1.283547257876313e-3
allele num: 8570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 3.154005587095612e-4
allele num: 66582
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.232142857142857e-3
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 20
allele frequency: 1.246571927200199e-3
allele num: 16044
num of homozygotes: 5

African
type: Population
allele count: 7
allele frequency: 7.217983089296762e-4
allele num: 9698
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.17e-1

FS
type: SiteQuality
SIO_000300: 2.8848e1

VQSLOD
type: SiteQuality
SIO_000300: 1.019e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: -1.929e0

QD
type: SiteQuality
SIO_000300: 6.38e0

DP
type: SiteQuality
SIO_000300: 1.1286924e7

MQ
type: SiteQuality
SIO_000300: 4.331e1

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54632
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2260
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16178
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.159e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.71e-1

MQ
type: SiteQuality
SIO_000300: 5.162e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.18e-1

FS
type: SiteQuality
SIO_000300: 7.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.532999999999999e0

DP
type: SiteQuality
SIO_000300: 1.1282431e7

QD
type: SiteQuality
SIO_000300: 1.32e1

GenotypeQuality
all individuals: 771
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2121
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 257
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54632
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 1
allele frequency: 6.178178672927221e-5
allele num: 16186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 5.056e1

MQRankSum
type: SiteQuality
SIO_000300: -4.16e-1

FS
type: SiteQuality
SIO_000300: 1.7243e1

VQSLOD
type: SiteQuality
SIO_000300: -4.583e0

QD
type: SiteQuality
SIO_000300: 1.284e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

DP
type: SiteQuality
SIO_000300: 1.1280969e7

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.961e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.949999999999999e0

GenotypeQuality
all individuals: 218
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54629
bin: 9.75e1
variant carriers: 338

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 144
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 332
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 367
allele frequency: 3.781166288893468e-2
allele num: 9706
num of homozygotes: 35

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.502611514678514e-5
allele num: 66628
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.732099196646874e-4
allele num: 11452
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16172
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.732e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.017e1

MQ
type: SiteQuality
SIO_000300: 5.219e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.1291617e7

FS
type: SiteQuality
SIO_000300: 5.096e0

QD
type: SiteQuality
SIO_000300: 1.444e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e-1

GenotypeQuality
all individuals: 97
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2154
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54629
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16172
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.1291617e7

FS
type: SiteQuality
SIO_000300: 5.096e0

VQSLOD
type: SiteQuality
SIO_000300: 1.017e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.732e-1

QD
type: SiteQuality
SIO_000300: 1.444e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQ
type: SiteQuality
SIO_000300: 5.219e1

GenotypeQuality
all individuals: 517
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2035
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 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: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.856205915109516e-4
allele num: 16162
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.299e1

DP
type: SiteQuality
SIO_000300: 1.1270991e7

MQRankSum
type: SiteQuality
SIO_000300: 6.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.824e0

FS
type: SiteQuality
SIO_000300: 6.283e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 5.214e1

GenotypeQuality
all individuals: 315
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54620
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1713
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16146
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.85e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

MQ
type: SiteQuality
SIO_000300: 5.03e1

FS
type: SiteQuality
SIO_000300: 1.324e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.94e0

VQSLOD
type: SiteQuality
SIO_000300: -1.22e0

MQRankSum
type: SiteQuality
SIO_000300: -3.06e-1

DP
type: SiteQuality
SIO_000300: 1.1265981e7

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

GenotypeQuality
all individuals: 49
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 472
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 8.75e1
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: 66564
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

South Asian
type: Population
allele count: 21
allele frequency: 1.311188811188811e-3
allele num: 16016
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.176e0

QD
type: SiteQuality
SIO_000300: 1.356e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

DP
type: SiteQuality
SIO_000300: 1.1260169e7

MQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

FS
type: SiteQuality
SIO_000300: 9.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.723e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.65e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

MQ
type: SiteQuality
SIO_000300: 4.9e1

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.230151650312221e-4
allele num: 4484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1526
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.63e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.09e0

QD
type: SiteQuality
SIO_000300: 5.68e0

DP
type: SiteQuality
SIO_000300: 4.27997e5

MQ
type: SiteQuality
SIO_000300: 2.917e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.723e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.05e-1

GenotypeQuality
all individuals: 763
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2525
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.376651982378855e-4
allele num: 7264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1526
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4484
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

MQ
type: SiteQuality
SIO_000300: 2.917e1

VQSLOD
type: SiteQuality
SIO_000300: -4.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.723e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.63e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.05e-1

QD
type: SiteQuality
SIO_000300: 5.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.05e-1

DP
type: SiteQuality
SIO_000300: 4.27997e5

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 365
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3056
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1088
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 885
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31577
bin: 2.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.115264797507788e-3
allele num: 642
num of homozygotes: 0

African
type: Population
allele count: 18
allele frequency: 1.067615658362989e-2
allele num: 1686
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.231146809460062e-4
allele num: 4482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.63e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 2.989e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.145e1

DP
type: SiteQuality
SIO_000300: 4.74287e5

GenotypeQuality
all individuals: 298
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1067
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 509
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1008
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.05241001894338e-4
allele num: 9502
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.034e0

DP
type: SiteQuality
SIO_000300: 5.05903e5

QD
type: SiteQuality
SIO_000300: 1.132e1

VQSLOD
type: SiteQuality
SIO_000300: -4.139e0

MQ
type: SiteQuality
SIO_000300: 3.061e1

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.96e-2