7-6452417-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452417
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452417
    reference: chr 7
allele count: 2
allele frequency: 6.821282401091406e-5
allele num: 29320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.252G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1182+25G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*7+25G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1428+25G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1446+25G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1221+25G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1569+25G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25127
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1170
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2106
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 17460
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/7-6452421-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452421
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452421
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 30090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1446+21G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1428+21G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1221+21G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*7+21G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.248G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1569+21G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1182+21G>T
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26380
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18089
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16358
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/7-6452423-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452423
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452423
    reference: chr 7
allele count: 28
allele frequency: 9.20568122041031e-4
allele num: 30416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1221+19G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1428+19G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1446+19G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1569+19G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.246G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1182+19G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*7+19G>T
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26994
  bin: 7.5e0
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15791
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23202
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6135
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP

7-6452429-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452429
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452429
    reference: chr 7
allele count: 1
allele frequency: 3.154375118289067e-5
allele num: 31702
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1446+13C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1428+13C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1221+13C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1569+13C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*7+13C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1182+13C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.240C>G
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14872
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1833
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13858
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26011
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS

7-6452431-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452431
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452431
    reference: chr 7
allele count: 1
allele frequency: 3.090616887130671e-5
allele num: 32356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1428+11G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1221+11G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1569+11G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1446+11G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1182+11G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.238G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*7+11G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13298
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2106
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6515
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1667
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/7-6452434-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452434
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452434
    reference: chr 7
allele count: 2
allele frequency: 5.996282304970918e-5
allele num: 33354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1221+8G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1182+8G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1428+8G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1569+8G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1446+8G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*7+8G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.235G>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4056
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27496
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2107
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1397
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
hgvs: c.1569+8G>T
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD

7-6452435-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452435
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452435
    reference: chr 7
allele count: 1
allele frequency: 2.967887457707604e-5
allele num: 33694
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.234G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1428+7G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1446+7G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1221+7G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1569+7G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*7+7G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1182+7G>C
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1769
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6855
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
hgvs: c.1569+7G>C
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ

7-6452435-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452435
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452435
    reference: chr 7
allele count: 73
allele frequency: 2.166557844126551e-3
allele num: 33694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1221+7G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.234G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1569+7G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1182+7G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*7+7G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1428+7G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1446+7G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 30222
  bin: 7.5e0
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12715
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 1.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 9.75e1
  variant carriers: 72
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 7.25e1
  variant carriers: 3
hgvs: c.1569+7G>A
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

7-6452436-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452436
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452436
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 34258
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1569+6C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.233C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*7+6C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1182+6C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1428+6C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1221+6C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1446+6C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30577
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28019
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6950
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1379
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 9.75e1
  variant carriers: 1
hgvs: c.1569+6C>T
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

7-6452437-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452437
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452437
    reference: chr 7
allele count: 1
allele frequency: 2.872572676088705e-5
allele num: 34812
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1221+5G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*7+5G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1569+5G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.232G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1446+5G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1182+5G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1428+5G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30845
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11787
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7154
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1742
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1569+5G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

7-6452443-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452443
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452443
    reference: chr 7
allele count: 1
allele frequency: 2.730748225013654e-5
allele num: 36620
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1220A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1181A>G
  hgvsp: ENSP00000391171.2:p.Lys394Arg
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*6A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1568A>G
  hgvsp: ENSP00000297056.6:p.Lys523Arg
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1445A>G
  hgvsp: ENSP00000404785.1:p.Lys482Arg
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.226A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1427A>G
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9885
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31985
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2106
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1872
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29416
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7476
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys523Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum

7-6452447-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452447
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452447
    reference: chr 7
allele count: 1
allele frequency: 2.633242047609016e-5
allele num: 37976
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*2C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.222C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1177C>T
  hgvsp: ENSP00000391171.2:p.Pro393Ser
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1216C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1564C>T
  hgvsp: ENSP00000297056.6:p.Pro522Ser
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1441C>T
  hgvsp: ENSP00000404785.1:p.Pro481Ser
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1423C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8930
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32258
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1912
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1429
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8571
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1067
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro522Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

7-6452447-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452447
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452448
    reference: chr 7
allele count: 1
allele frequency: 2.633242047609016e-5
allele num: 37976
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1215dupA
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1563dupA
  hgvsp: ENSP00000297056.6:p.Pro522ThrfsTer96
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1440dupA
  hgvsp: ENSP00000404785.1:p.Pro481ThrfsTer96
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.*1dupA
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1176dupA
  hgvsp: ENSP00000391171.2:p.Pro393ThrfsTer96
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.221dupA
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1422dupA
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8930
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1912
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1067
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro522ThrfsTer96
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

7-6452452-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452452
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452452
    reference: chr 7
allele count: 3
allele frequency: 7.575757575757576e-5
allele num: 39600
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1211A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1137A>G
  hgvsp: ENST00000428902.2:c.1137A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1418A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.217A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1559A>G
  hgvsp: ENSP00000297056.6:p.Asn520Ser
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1436A>G
  hgvsp: ENSP00000404785.1:p.Asn479Ser
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1172A>G
  hgvsp: ENSP00000391171.2:p.Asn391Ser
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32679
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7822
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1449
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30725
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn520Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

7-6452453-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452453
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452453
    reference: chr 7
allele count: 1
allele frequency: 2.507019655034095e-5
allele num: 39888
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.216A>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1136A>C
  hgvsp: ENSP00000416046.2:p.Gln379Pro
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1171A>C
  hgvsp: ENSP00000391171.2:p.Asn391His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1210A>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1558A>C
  hgvsp: ENSP00000297056.6:p.Asn520His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1435A>C
  hgvsp: ENSP00000404785.1:p.Asn479His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1417A>C
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8570
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1788
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn520His
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD

7-6452454-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452454
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452454
    reference: chr 7
allele count: 1
allele frequency: 2.484595507851322e-5
allele num: 40248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1135C>T
  hgvsp: ENSP00000416046.2:p.Gln379Ter
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1209C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.215C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1170C>T
  hgvsp: ENST00000425398.2:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1434C>T
  hgvsp: ENST00000436575.1:c.1434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1416C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1557C>T
  hgvsp: ENST00000297056.6:c.1557C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln379Ter
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

7-6452458-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452458
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452458
    reference: chr 7
allele count: 1
allele frequency: 2.363172322525759e-5
allele num: 42316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1166A>C
  hgvsp: ENSP00000391171.2:p.His389Pro
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1205A>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1131A>C
  hgvsp: ENST00000428902.2:c.1131A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1553A>C
  hgvsp: ENSP00000297056.6:p.His518Pro
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1412A>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.211A>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1430A>C
  hgvsp: ENSP00000404785.1:p.His477Pro
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2064
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2107
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6198
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His518Pro
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

7-6452460-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452460
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452460
    reference: chr 7
allele count: 1
allele frequency: 2.324716384601079e-5
allele num: 43016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1164G>A
  hgvsp: ENST00000425398.2:c.1164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.209G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1129G>A
  hgvsp: ENSP00000416046.2:p.Ala377Thr
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1551G>A
  hgvsp: ENST00000297056.6:c.1551G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1203G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1410G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1428G>A
  hgvsp: ENST00000436575.1:c.1428G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32543
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1848
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8901
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2108
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2249
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala377Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum

7-6452461-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452461
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452461
    reference: chr 7
allele count: 3081
allele frequency: 6.59771296415264e-2
allele num: 46698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.208C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1427C>T
  hgvsp: ENSP00000404785.1:p.Ala476Val
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1163C>T
  hgvsp: ENSP00000391171.2:p.Ala388Val
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1550C>T
  hgvsp: ENSP00000297056.6:p.Ala517Val
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1128C>T
  hgvsp: ENST00000428902.2:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1409C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1202C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 2.25e1
  variant carriers: 260
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 1.75e1
  variant carriers: 676
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 2.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.75e1
  variant carriers: 506
genotype depth: GenotypeDepth
  all individuals: 6218
  bin: 1.25e1
  variant carriers: 953
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 2.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 31361
  bin: 7.5e0
  variant carriers: 526
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 3.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.25e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 4.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 5149
  bin: 7.5e0
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 5.75e1
  variant carriers: 43
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 7.75e1
  variant carriers: 77
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 8.25e1
  variant carriers: 81
genotype quality: GenotypeQuality
  all individuals: 4485
  bin: 9.75e1
  variant carriers: 2758
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 2.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 1777
  bin: 3.25e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 29393
  bin: 2.25e1
  variant carriers: 29
hgvs: p.Ala517Val
num of homozygotes: 90
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

7-6452462-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452462
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452462
    reference: chr 7
allele count: 5
allele frequency: 1.054229569030952e-4
allele num: 47428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1201G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1549G>A
  hgvsp: ENSP00000297056.6:p.Ala517Thr
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1162G>A
  hgvsp: ENSP00000391171.2:p.Ala388Thr
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1127G>A
  hgvsp: ENSP00000416046.2:p.Arg376His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.207G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1408G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1426G>A
  hgvsp: ENSP00000404785.1:p.Ala476Thr
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31239
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6954
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2204
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5032
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala517Thr
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

7-6452463-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452463
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452463
    reference: chr 7
allele count: 32
allele frequency: 6.550933508024893e-4
allele num: 48848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1407C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1161C>T
  hgvsp: ENST00000425398.2:c.1161C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.206C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1425C>T
  hgvsp: ENST00000436575.1:c.1425C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1548C>T
  hgvsp: ENST00000297056.6:c.1548C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1200C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1126C>T
  hgvsp: ENSP00000416046.2:p.Arg376Cys
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30990
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6501
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7494
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30475
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1628
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg376Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

7-6452467-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452467
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452467
    reference: chr 7
allele count: 1
allele frequency: 1.927153594141453e-5
allele num: 51890
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1403T>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.202T>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1421T>A
  hgvsp: ENSP00000404785.1:p.Val474Glu
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1544T>A
  hgvsp: ENSP00000297056.6:p.Val515Glu
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1157T>A
  hgvsp: ENSP00000391171.2:p.Val386Glu
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1122T>A
  hgvsp: ENSP00000416046.2:p.Ser374Arg
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1196T>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30289
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2317
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val515Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ

7-6452470-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452470
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452470
    reference: chr 7
allele count: 8
allele frequency: 1.498632497845716e-4
allele num: 53382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.199G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1400G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1541G>A
  hgvsp: ENSP00000297056.6:p.Arg514Gln
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1193G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1119G>A
  hgvsp: ENST00000428902.2:c.1119G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1154G>A
  hgvsp: ENSP00000391171.2:p.Arg385Gln
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1418G>A
  hgvsp: ENSP00000404785.1:p.Arg473Gln
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30000
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6741
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9183
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2429
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29948
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12372
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 8.75e1
  variant carriers: 1
hgvs: p.Arg514Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

7-6452471-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452471
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452471
    reference: chr 7
allele count: 5
allele frequency: 9.195909659383507e-5
allele num: 54372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1399C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.198C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1540C>G
  hgvsp: ENSP00000297056.6:p.Arg514Gly
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1417C>G
  hgvsp: ENSP00000404785.1:p.Arg473Gly
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1118C>G
  hgvsp: ENSP00000416046.2:p.Ala373Gly
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1153C>G
  hgvsp: ENSP00000391171.2:p.Arg385Gly
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1192C>G
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6802
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29743
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1857
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2459
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1711
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg514Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/7-6452476-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452476
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452476
    reference: chr 7
allele count: 6
allele frequency: 1.03280889592729e-4
allele num: 58094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1187T>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1394T>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1535T>G
  hgvsp: ENSP00000297056.6:p.Ile512Ser
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.193T>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1148T>G
  hgvsp: ENSP00000391171.2:p.Ile383Ser
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1113T>G
  hgvsp: ENSP00000416046.2:p.Asn371Lys
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1412T>G
  hgvsp: ENSP00000404785.1:p.Ile471Ser
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28846
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29208
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2436
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2552
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile512Ser
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

7-6452479-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452479
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452479
    reference: chr 7
allele count: 1
allele frequency: 1.687877662627013e-5
allele num: 59246
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1145G>C
  hgvsp: ENSP00000391171.2:p.Arg382Thr
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1409G>C
  hgvsp: ENSP00000404785.1:p.Arg470Thr
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1184G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1110G>C
  hgvsp: ENSP00000416046.2:p.Lys370Asn
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1532G>C
  hgvsp: ENSP00000297056.6:p.Arg511Thr
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1391G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.190G>C
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2340
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14424
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg511Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-6452492-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452492
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452492
    reference: chr 7
allele count: 3
allele frequency: 4.592211609110948e-5
allele num: 65328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1132G>T
  hgvsp: ENSP00000391171.2:p.Asp378Tyr
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1097G>T
  hgvsp: ENSP00000416046.2:p.Arg366Ile
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.177G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1396G>T
  hgvsp: ENSP00000404785.1:p.Asp466Tyr
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1378G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1519G>T
  hgvsp: ENSP00000297056.6:p.Asp507Tyr
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1171G>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1549
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27036
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp507Tyr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD

7-6452492-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452492
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452492
    reference: chr 7
allele count: 1
allele frequency: 1.530737203036983e-5
allele num: 65328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1171G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1097G>A
  hgvsp: ENSP00000416046.2:p.Arg366Lys
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1132G>A
  hgvsp: ENSP00000391171.2:p.Asp378Asn
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.177G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1519G>A
  hgvsp: ENSP00000297056.6:p.Asp507Asn
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1396G>A
  hgvsp: ENSP00000404785.1:p.Asp466Asn
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1378G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13040
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2631
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16213
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp507Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

7-6452511-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452511
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452511
    reference: chr 7
allele count: 1
allele frequency: 1.326084073730275e-5
allele num: 75410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1078C>T
  hgvsp: ENSP00000416046.2:p.Gln360Ter
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1152C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1377C>T
  hgvsp: ENST00000436575.1:c.1377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1113C>T
  hgvsp: ENST00000425398.2:c.1113C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1359C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.158C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1500C>T
  hgvsp: ENST00000297056.6:c.1500C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7383
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21779
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2829
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2677
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln360Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum

7-6452513-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452513
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452513
    reference: chr 7
allele count: 10
allele frequency: 1.309723386420788e-4
allele num: 76352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1357C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1375C>T
  hgvsp: ENSP00000404785.1:p.Leu459Phe
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1498C>T
  hgvsp: ENSP00000297056.6:p.Leu500Phe
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1111C>T
  hgvsp: ENSP00000391171.2:p.Leu371Phe
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1076C>T
  hgvsp: ENSP00000416046.2:p.Ala359Val
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.156C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1150C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16296
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7393
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5918
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22861
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18884
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2878
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu500Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

7-6452515-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452515
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452515
    reference: chr 7
allele count: 1
allele frequency: 1.284950657894737e-5
allele num: 77824
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1497-1G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1075-1G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1149-1G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1356-1G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1110-1G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.155-1G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1374-1G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2659
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1027
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 3.75e1
  variant carriers: 0
hgvs: c.1497-1G>A
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

7-6452529-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452529
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452529
    reference: chr 7
allele count: 2
allele frequency: 2.338032779219565e-5
allele num: 85542
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1497-15C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1110-15C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1149-15C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.155-15C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1075-15C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1374-15C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1356-15C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18666
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1831
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3130
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1761
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2738
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/7-6452535-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452535
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452535
    reference: chr 7
allele count: 2
allele frequency: 2.255503428365211e-5
allele num: 88672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.155-21G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1356-21G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1497-21G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1149-21G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1110-21G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1374-21G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1075-21G>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2656
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3068
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2197
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-6452537-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452537
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452537
    reference: chr 7
allele count: 1
allele frequency: 1.114081996434938e-5
allele num: 89760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1075-23C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1374-23C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1497-23C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1110-23C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1149-23C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.155-23C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1356-23C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3037
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2637
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

7-6452547-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452547
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452547
    reference: chr 7
allele count: 1
allele frequency: 1.054563094509945e-5
allele num: 94826
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1075-33G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1110-33G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.155-33G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1374-33G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1356-33G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1497-33G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1149-33G>C
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8187
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14597
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1848
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

7-6452551-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452551
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452551
    reference: chr 7
allele count: 1
allele frequency: 1.032865789419323e-5
allele num: 96818
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1497-37C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1356-37C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1374-37C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.155-37C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1110-37C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1075-37C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1149-37C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2495
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1572
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2753
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/7-6452554-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452554
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452554
    reference: chr 7
allele count: 1
allele frequency: 1.013027534088376e-5
allele num: 98714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1110-40G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.155-40G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1075-40G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1497-40G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1149-40G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1356-40G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1374-40G>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5074
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28543
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2315
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2685
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12710
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-6452560-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452560
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452559
    reference: chr 7
allele count: 4
allele frequency: 3.926881467082916e-5
allele num: 101862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1074+36delG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1373+36delG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1496+36delG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1109+36delG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1355+36delG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.154+36delG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1148+36delG
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9967
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2736
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32180
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1837
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: AC
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/7-6452562-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452562
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452562
    reference: chr 7
allele count: 1
allele frequency: 9.679417686231996e-6
allele num: 103312
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1496+35G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.154+35G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1148+35G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1109+35G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1074+35G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1355+35G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1373+35G>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10397
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10078
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

7-6452562-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452562
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452562
    reference: chr 7
allele count: 1
allele frequency: 9.679417686231996e-6
allele num: 103312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1074+35G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1148+35G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1109+35G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1496+35G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1373+35G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1355+35G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.154+35G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10397
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

7-6452566-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452566
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452566
    reference: chr 7
allele count: 34
allele frequency: 3.209060877772534e-4
allele num: 105950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1109+31G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.154+31G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1496+31G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1148+31G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1373+31G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1074+31G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1355+31G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11144
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29115
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7330
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35427
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS

http://identifiers.org/exac.variant/7-6452566-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452566
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452566
    reference: chr 7
allele count: 2
allele frequency: 1.887682869277961e-5
allele num: 105950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1148+31G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1074+31G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1496+31G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1109+31G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1355+31G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.154+31G>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1373+31G>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1880
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1903
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

7-6452572-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452572
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452572
    reference: chr 7
allele count: 2
allele frequency: 1.825217200846901e-5
allele num: 109576
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1074+25A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1148+25A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.154+25A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1373+25A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1109+25A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1355+25A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1496+25A>G
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

7-6452578-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452578
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452578
    reference: chr 7
allele count: 21
allele frequency: 1.87885836986669e-4
allele num: 111770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.154+19G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1109+19G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1496+19G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1148+19G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1074+19G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1355+19G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1373+19G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33431
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12718
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5554
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

7-6452583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452583
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452583
    reference: chr 7
allele count: 1
allele frequency: 8.825657952800381e-6
allele num: 113306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1373+14G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1074+14G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.154+14G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1148+14G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1109+14G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1496+14G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1355+14G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-6452584-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452584
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452584
    reference: chr 7
allele count: 9
allele frequency: 7.926721860137397e-5
allele num: 113540
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1373+13G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1109+13G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1148+13G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1074+13G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.154+13G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1355+13G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1496+13G>C
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13278
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34671
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4487
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff

7-6452585-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452585
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452585
    reference: chr 7
allele count: 98
allele frequency: 8.606758940490409e-4
allele num: 113864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.154+12T>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1074+12T>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1355+12T>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1109+12T>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1373+12T>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1148+12T>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1496+12T>C
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13347
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34784
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3530
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44448
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

7-6452587-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452587
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452587
    reference: chr 7
allele count: 18
allele frequency: 1.574610283954721e-4
allele num: 114314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.154+10C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1109+10C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1373+10C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1148+10C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1496+10C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1074+10C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1355+10C>G
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35058
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13535
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 9.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4085
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

7-6452598-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452598
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452598
    reference: chr 7
allele count: 1
allele frequency: 8.620689655172414e-6
allele num: 116000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.153A>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1073A>T
  hgvsp: ENSP00000416046.2:p.Gln358Leu
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1354A>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1147A>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1495A>T
  hgvsp: ENSP00000297056.6:p.Arg499Trp
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1108A>T
  hgvsp: ENSP00000391171.2:p.Arg370Trp
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1372A>T
  hgvsp: ENSP00000404785.1:p.Arg458Trp
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14335
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3167
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg499Trp
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/7-6452606-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452606
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452606
    reference: chr 7
allele count: 4
allele frequency: 3.427004797806717e-5
allele num: 116720
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1346T>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1139T>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1065T>G
  hgvsp: ENSP00000416046.2:p.Cys355Trp
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1100T>G
  hgvsp: ENSP00000391171.2:p.Val367Gly
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1364T>G
  hgvsp: ENSP00000404785.1:p.Val455Gly
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.145T>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1487T>G
  hgvsp: ENSP00000297056.6:p.Val496Gly
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14802
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2774
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3719
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val496Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

7-6452610-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452610
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452610
    reference: chr 7
allele count: 1
allele frequency: 8.551393877201984e-6
allele num: 116940
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1096G>C
  hgvsp: ENSP00000391171.2:p.Asp366His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1483G>C
  hgvsp: ENSP00000297056.6:p.Asp495His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1360G>C
  hgvsp: ENSP00000404785.1:p.Asp454His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.141G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1061G>C
  hgvsp: ENSP00000416046.2:p.Gly354Ala
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1135G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1342G>C
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2638
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3735
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1837
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asp495His
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

7-6452619-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452619
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452619
    reference: chr 7
allele count: 1
allele frequency: 8.505137102810097e-6
allele num: 117576
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1052C>A
  hgvsp: ENSP00000416046.2:p.Pro351His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*764C>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1087C>A
  hgvsp: ENSP00000391171.2:p.Leu363Met
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.132C>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1351C>A
  hgvsp: ENSP00000404785.1:p.Leu451Met
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1126C>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1474C>A
  hgvsp: ENSP00000297056.6:p.Leu492Met
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1333C>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*411C>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2334
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu492Met
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

7-6452620-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452620
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452620
    reference: chr 7
allele count: 1
allele frequency: 8.499498529586754e-6
allele num: 117654
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1473C>T
  hgvsp: ENST00000297056.6:c.1473C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*410C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1350C>T
  hgvsp: ENST00000436575.1:c.1350C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1086C>T
  hgvsp: ENST00000425398.2:c.1086C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1051C>T
  hgvsp: ENSP00000416046.2:p.Pro351Ser
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1125C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*763C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.131C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1332C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48433
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro351Ser
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

7-6452622-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452622
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452622
    reference: chr 7
allele count: 3
allele frequency: 2.550022950206552e-5
allele num: 117646
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*408G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1049G>C
  hgvsp: ENSP00000416046.2:p.Arg350Pro
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1330G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.129G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1084G>C
  hgvsp: ENSP00000391171.2:p.Val362Leu
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*761G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1348G>C
  hgvsp: ENSP00000404785.1:p.Val450Leu
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1471G>C
  hgvsp: ENSP00000297056.6:p.Val491Leu
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1123G>C
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47953
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val491Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

7-6452622-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452622
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452622
    reference: chr 7
allele count: 8
allele frequency: 6.800061200550805e-5
allele num: 117646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1084G>A
  hgvsp: ENSP00000391171.2:p.Val362Ile
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1123G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1049G>A
  hgvsp: ENSP00000416046.2:p.Arg350His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1471G>A
  hgvsp: ENSP00000297056.6:p.Val491Ile
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*408G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*761G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1348G>A
  hgvsp: ENSP00000404785.1:p.Val450Ile
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1330G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.129G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36072
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3714
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val491Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

7-6452623-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452623
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452623
    reference: chr 7
allele count: 4
allele frequency: 3.398066500161408e-5
allele num: 117714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1048C>T
  hgvsp: ENSP00000416046.2:p.Arg350Cys
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*760C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1122C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1083C>T
  hgvsp: ENST00000425398.2:c.1083C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.128C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*407C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1329C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1347C>T
  hgvsp: ENST00000436575.1:c.1347C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1470C>T
  hgvsp: ENST00000297056.6:c.1470C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36111
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg350Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP

7-6452631-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452631
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452631
    reference: chr 7
allele count: 8
allele frequency: 6.797172376291462e-5
allele num: 117696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*399G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1321G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*752G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.120G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1075G>A
  hgvsp: ENSP00000391171.2:p.Val359Met
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1040G>A
  hgvsp: ENSP00000416046.2:p.Arg347His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1462G>A
  hgvsp: ENSP00000297056.6:p.Val488Met
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1114G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1339G>A
  hgvsp: ENSP00000404785.1:p.Val447Met
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15701
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val488Met
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

7-6452632-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452632
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452632
    reference: chr 7
allele count: 2
allele frequency: 1.699004383431309e-5
allele num: 117716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1338C>T
  hgvsp: ENST00000436575.1:c.1338C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1074C>T
  hgvsp: ENST00000425398.2:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1039C>T
  hgvsp: ENSP00000416046.2:p.Arg347Cys
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1320C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.119C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1113C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1461C>T
  hgvsp: ENST00000297056.6:c.1461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*398C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*751C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35783
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3671
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg347Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

7-6452632-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452632
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452632
    reference: chr 7
allele count: 3
allele frequency: 2.548506575146964e-5
allele num: 117716
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1320C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*398C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*751C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1074C>G
  hgvsp: ENSP00000391171.2:p.Ile358Met
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1039C>G
  hgvsp: ENSP00000416046.2:p.Arg347Gly
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1113C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1461C>G
  hgvsp: ENSP00000297056.6:p.Ile487Met
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1338C>G
  hgvsp: ENSP00000404785.1:p.Ile446Met
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.119C>G
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile487Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

7-6452649-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452649
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452649
    reference: chr 7
allele count: 1
allele frequency: 8.58000858000858e-6
allele num: 116550
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1057T>C
  hgvsp: ENSP00000391171.2:p.Tyr353His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.102T>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1022T>C
  hgvsp: ENSP00000416046.2:p.Ile341Thr
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1444T>C
  hgvsp: ENSP00000297056.6:p.Tyr482His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1303T>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1321T>C
  hgvsp: ENSP00000404785.1:p.Tyr441His
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*381T>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*734T>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1096T>C
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Tyr482His
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

7-6452652-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452652
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452652
    reference: chr 7
allele count: 1
allele frequency: 8.59697386519945e-6
allele num: 116320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*378G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1019G>A
  hgvsp: ENSP00000416046.2:p.Gly340Glu
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.99G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1441G>A
  hgvsp: ENSP00000297056.6:p.Glu481Lys
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1054G>A
  hgvsp: ENSP00000391171.2:p.Glu352Lys
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*731G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1318G>A
  hgvsp: ENSP00000404785.1:p.Glu440Lys
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1300G>A
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1093G>A
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45873
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu481Lys
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

7-6452660-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452660
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452660
    reference: chr 7
allele count: 1
allele frequency: 8.66145824310981e-6
allele num: 115454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1292C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1046C>T
  hgvsp: ENSP00000391171.2:p.Ala349Val
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1085C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1011C>T
  hgvsp: ENST00000428902.2:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*370C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.91C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*723C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1310C>T
  hgvsp: ENSP00000404785.1:p.Ala437Val
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1433C>T
  hgvsp: ENSP00000297056.6:p.Ala478Val
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32478
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1839
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5031
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala478Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

7-6452665-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452665
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452665
    reference: chr 7
allele count: 2
allele frequency: 1.740916766769381e-5
allele num: 114882
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1428C>T
  hgvsp: ENST00000297056.6:c.1428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.86C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1287C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1006C>T
  hgvsp: ENSP00000416046.2:p.Gln336Ter
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1080C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1305C>T
  hgvsp: ENST00000436575.1:c.1305C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1041C>T
  hgvsp: ENST00000425398.2:c.1041C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*718C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*365C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14765
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln336Ter
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

7-6452674-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452674
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452674
    reference: chr 7
allele count: 1
allele frequency: 8.813523470413002e-6
allele num: 113462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1287-9G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.86-9G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1006-9G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1041-9G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*718-9G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1428-9G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*365-9G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1305-9G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1080-9G>C
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2888
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/7-6452674-CCAAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452674
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452670
    reference: chr 7
allele count: 14
allele frequency: 1.23389328585782e-4
allele num: 113462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1080-13_1080-10delTTTG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.86-13_86-10delTTTG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*718-13_*718-10delTTTG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1006-13_1006-10delTTTG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1428-13_1428-10delTTTG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*365-13_*365-10delTTTG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1305-13_1305-10delTTTG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1287-13_1287-10delTTTG
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1041-13_1041-10delTTTG
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 28477
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14180
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7107
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7856
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39983
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 14
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: CCAAA
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD

7-6452679-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452679
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452679
    reference: chr 7
allele count: 21
allele frequency: 1.864975755315181e-4
allele num: 112602
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1041-14G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1287-14G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1305-14G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1080-14G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1428-14G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*365-14G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1006-14G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.86-14G>C
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*718-14G>C
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13704
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26056
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum

7-6452681-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452681
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452681
    reference: chr 7
allele count: 285
allele frequency: 2.54096752910968e-3
allele num: 112162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1287-16C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1305-16C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*365-16C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1080-16C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*718-16C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1006-16C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1041-16C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.86-16C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1428-16C>G
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10767
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 13156
  bin: 2.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24295
  bin: 2.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 1.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 3.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 3.25e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10216
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2551
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 5
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

7-6452683-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452683
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452683
    reference: chr 7
allele count: 1
allele frequency: 8.932878352062602e-6
allele num: 111946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.86-18C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1006-18C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*365-18C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1287-18C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1428-18C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1080-18C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1041-18C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*718-18C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1305-18C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12962
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2573
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-6452685-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452685
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452685
    reference: chr 7
allele count: 4
allele frequency: 3.587443946188341e-5
allele num: 111500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*718-20C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1006-20C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1041-20C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1287-20C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.86-20C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1428-20C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1080-20C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1305-20C>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*365-20C>G
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21491
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4562
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2228
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3928
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

7-6452692-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452692
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452692
    reference: chr 7
allele count: 1
allele frequency: 9.06059727457234e-6
allele num: 110368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1305-27A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1080-27A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1287-27A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1006-27A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1428-27A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*718-27A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.86-27A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1041-27A>G
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*365-27A>G
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

7-6452695-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6452695
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 6452695
    reference: chr 7
allele count: 1
allele frequency: 9.125752874612156e-6
allele num: 109580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000408928
  ensembl transcript: ENST00000421761
  gene symbol: DAGLB
  hgvsc: ENST00000421761.2:c.*365-30C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000482149
  gene symbol: DAGLB
  hgvsc: ENST00000482149.1:n.1080-30C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000462934
  gene symbol: DAGLB
  hgvsc: ENST00000462934.1:n.1287-30C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000391171
  ensembl transcript: ENST00000425398
  gene symbol: DAGLB
  hgvsc: ENST00000425398.2:c.1041-30C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl transcript: ENST00000497308
  gene symbol: DAGLB
  hgvsc: ENST00000497308.1:n.86-30C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000411746
  ensembl transcript: ENST00000454738
  gene symbol: DAGLB
  hgvsc: ENST00000454738.1:c.*718-30C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000297056
  ensembl transcript: ENST00000297056
  gene symbol: DAGLB
  hgvsc: ENST00000297056.6:c.1428-30C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000404785
  ensembl transcript: ENST00000436575
  gene symbol: DAGLB
  hgvsc: ENST00000436575.1:c.1305-30C>T
  variant of: http://identifiers.org/hgnc/28923
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164535
  ensembl protein: ENSP00000416046
  ensembl transcript: ENST00000428902
  gene symbol: DAGLB
  hgvsc: ENST00000428902.2:c.1006-30C>T
  variant of: http://identifiers.org/hgnc/28923
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13877
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7460
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5008
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G

GenotypeQuality
all individuals: 2957
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5931
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2274
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21359
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.679528403001072e-4
allele num: 3732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.453786523553965e-5
allele num: 13416
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8824
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 4.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.22e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.407e1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 6.47655e5

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

GenotypeQuality
all individuals: 478
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2535
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22340
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6036
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2106
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1748
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8900
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-2

QD
type: SiteQuality
SIO_000300: 2.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.791e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

DP
type: SiteQuality
SIO_000300: 6.59481e5

GenotypeQuality
all individuals: 2357
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 392
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 482
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1257
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 9.75e1
variant carriers: 28

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 1

South Asian
type: Population
allele count: 3
allele frequency: 3.360967958772126e-4
allele num: 8926
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3842
num of homozygotes: 0

East Asian
type: Population
allele count: 25
allele frequency: 1.363140676117775e-2
allele num: 1834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13988
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.95e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.186e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e0

QD
type: SiteQuality
SIO_000300: 1.004e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

FS
type: SiteQuality
SIO_000300: 6.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.6594e5

GenotypeQuality
all individuals: 1608
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6467
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1374
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2106
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 512
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1304
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14652
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.107174490699734e-4
allele num: 9032
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2010
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.54e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.73e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.63e-2

DP
type: SiteQuality
SIO_000300: 6.8641e5

FS
type: SiteQuality
SIO_000300: 3.022e0

GenotypeQuality
all individuals: 1385
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26191
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2297
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2092
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.657789613848202e-5
allele num: 15020
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9056
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1366
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

QD
type: SiteQuality
SIO_000300: 3.71e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.744e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.56e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.78e-1

DP
type: SiteQuality
SIO_000300: 6.92833e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.827e0

GenotypeQuality
all individuals: 12336
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.435834727764191e-5
allele num: 15538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4086
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.09217999126256e-4
allele num: 9156
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.282e0

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.55e-1

FS
type: SiteQuality
SIO_000300: 3.997e0

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.03246e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.37e-2

QD
type: SiteQuality
SIO_000300: 1.126e1

GenotypeQuality
all individuals: 485
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1947
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12012
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27604
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4106
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.087429317094389e-4
allele num: 9196
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.02e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

DP
type: SiteQuality
SIO_000300: 7.08812e5

QD
type: SiteQuality
SIO_000300: 1.245e1

VQSLOD
type: SiteQuality
SIO_000300: 5.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 514
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 210
bin: 8.75e1
variant carriers: 8

GenotypeQuality
all individuals: 12012
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6855
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1947
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1400
bin: 6.75e1
variant carriers: 6

GenotypeQuality
all individuals: 27604
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 493
bin: 3.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 1.087429317094389e-4
allele num: 9196
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4106
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 48
allele frequency: 3.053046686172243e-3
allele num: 15722
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 2.707581227436823e-3
allele num: 2216
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 7.761966364812419e-3
allele num: 1546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.900990099009901e-3
allele num: 606
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.02e-2

QD
type: SiteQuality
SIO_000300: 1.245e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

DP
type: SiteQuality
SIO_000300: 7.08812e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

GenotypeQuality
all individuals: 2006
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11520
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
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variant carriers: 0

GenotypeQuality
all individuals: 1392
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4164
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16006
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9220
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 7.14178e5

FS
type: SiteQuality
SIO_000300: 7.782e0

QD
type: SiteQuality
SIO_000300: 9.23e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.26e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.14e-1

GenotypeQuality
all individuals: 1288
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1847
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11197
bin: 7.5e0
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GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
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variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28652
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1686
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16290
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2404
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.079913606911447e-4
allele num: 9260
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.13e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 7.18285e5

FS
type: SiteQuality
SIO_000300: 1.328e0

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.322e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.773e-1

QD
type: SiteQuality
SIO_000300: 1.057e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.819e0

GenotypeQuality
all individuals: 9442
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1850
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.794414184725924e-5
allele num: 17258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2658
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-2

QD
type: SiteQuality
SIO_000300: 1.233e1

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

DP
type: SiteQuality
SIO_000300: 7.39187e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

GenotypeQuality
all individuals: 523
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 8.25e1
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GenotypeQuality
all individuals: 2106
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29679
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 4.25e1
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GenotypeQuality
all individuals: 2362
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7801
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17956
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.541076487252125e-4
allele num: 2824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2006
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.52286e5

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 6.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.56e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 7801
bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17956
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2824
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.985044865403788e-4
allele num: 2006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

QD
type: SiteQuality
SIO_000300: 6.99e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.56e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.52286e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 956
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2168
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.351206434316354e-4
allele num: 2984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.059322033898305e-4
allele num: 18880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

VQSLOD
type: SiteQuality
SIO_000300: 9.04e-1

QD
type: SiteQuality
SIO_000300: 1.206e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.62e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

DP
type: SiteQuality
SIO_000300: 7.67365e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.78e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4620
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.030078285949732e-4
allele num: 9708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19018
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 982
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.038e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

VQSLOD
type: SiteQuality
SIO_000300: -2.659e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

MQ
type: SiteQuality
SIO_000300: 5.864e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.59e-2

DP
type: SiteQuality
SIO_000300: 7.71018e5

MQRankSum
type: SiteQuality
SIO_000300: -1.426e0

QD
type: SiteQuality
SIO_000300: 1.993e1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.026904908605463e-4
allele num: 9738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2244
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 998
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3048
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.56e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.042e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.83e-1

FS
type: SiteQuality
SIO_000300: 2.069e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.3e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 7.74906e5

QD
type: SiteQuality
SIO_000300: 1.32e1

GenotypeQuality
all individuals: 9180
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 286
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GenotypeQuality
all individuals: 540
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3286
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.927079227433977e-5
allele num: 20296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9934
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

DP
type: SiteQuality
SIO_000300: 7.92476e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.362e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

QD
type: SiteQuality
SIO_000300: 1.192e1

GenotypeQuality
all individuals: 2093
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 538
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variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2560
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.001803245842517e-4
allele num: 9982
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1172
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4856
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

FS
type: SiteQuality
SIO_000300: 7.553e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.621e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.00993e5

QD
type: SiteQuality
SIO_000300: 8.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

GenotypeQuality
all individuals: 766
bin: 1.25e1
variant carriers: 22

GenotypeQuality
all individuals: 1618
bin: 1.75e1
variant carriers: 33

GenotypeQuality
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GenotypeQuality
all individuals: 254
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variant carriers: 98

GenotypeQuality
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variant carriers: 43

GenotypeQuality
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GenotypeQuality
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variant carriers: 95

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 36

GenotypeQuality
all individuals: 361
bin: 4.75e1
variant carriers: 54

East Asian
type: Population
allele count: 710
allele frequency: 1.696129956999522e-1
allele num: 4186
num of homozygotes: 33

African
type: Population
allele count: 213
allele frequency: 4.204500592183182e-2
allele num: 5066
num of homozygotes: 4

Other
type: Population
allele count: 19
allele frequency: 4.922279792746114e-2
allele num: 386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 39
allele frequency: 2.968036529680365e-2
allele num: 1314
num of homozygotes: 0

Latino
type: Population
allele count: 104
allele frequency: 3.680113234253362e-2
allele num: 2826
num of homozygotes: 1

South Asian
type: Population
allele count: 1079
allele frequency: 1.01124648547329e-1
allele num: 10670
num of homozygotes: 46

European (Non-Finnish)
type: Population
allele count: 917
allele frequency: 4.121348314606742e-2
allele num: 22250
num of homozygotes: 6

QD
type: SiteQuality
SIO_000300: 1.304e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 8.78459e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

FS
type: SiteQuality
SIO_000300: 5.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

GenotypeQuality
all individuals: 501
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2342
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GenotypeQuality
all individuals: 1862
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GenotypeQuality
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GenotypeQuality
all individuals: 342
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GenotypeQuality
all individuals: 482
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.321702352630188e-4
allele num: 22698
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 6.949270326615705e-4
allele num: 2878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4274
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.526e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

DP
type: SiteQuality
SIO_000300: 8.20895e5

VQSLOD
type: SiteQuality
SIO_000300: 7.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.27e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

FS
type: SiteQuality
SIO_000300: 4.317e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
all individuals: 362
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1109
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1877
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variant carriers: 26

GenotypeQuality
all individuals: 10941
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1468
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.281021897810219e-4
allele num: 4384
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 6.609385327164573e-4
allele num: 3026
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.922337562475971e-4
allele num: 5202
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.5e-3
allele num: 400
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.237021984112322e-5
allele num: 10826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 1.104409141109506e-3
allele num: 23542
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.21e-2

DP
type: SiteQuality
SIO_000300: 8.33488e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 5.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.35e0

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

QD
type: SiteQuality
SIO_000300: 1.195e1

GenotypeQuality
all individuals: 1002
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variant carriers: 0

GenotypeQuality
all individuals: 1855
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GenotypeQuality
all individuals: 2433
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GenotypeQuality
all individuals: 380
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GenotypeQuality
all individuals: 342
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3870
bin: 7.5e0
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11068
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.965107057890563e-5
allele num: 25220
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.42e0

FS
type: SiteQuality
SIO_000300: 2.187e0

VQSLOD
type: SiteQuality
SIO_000300: -3.091e0

QD
type: SiteQuality
SIO_000300: 2.05e0

DP
type: SiteQuality
SIO_000300: 8.54437e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 312
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3447
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1859
bin: 9.75e1
variant carriers: 7

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1699
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 3.072196620583717e-4
allele num: 26040
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4792
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11164
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.69661e5

FS
type: SiteQuality
SIO_000300: 1.126e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.307e0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

GenotypeQuality
all individuals: 164
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 504
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variant carriers: 1

GenotypeQuality
all individuals: 29709
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.126718245324119e-4
allele num: 26626
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 5.376344086021505e-4
allele num: 3720
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1868
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.77213e5

VQSLOD
type: SiteQuality
SIO_000300: -1.388e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.95e-1

FS
type: SiteQuality
SIO_000300: 1.021e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 2.933e1

GenotypeQuality
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 555
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1857
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 523
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5184
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 4.764173415912339e-4
allele num: 4198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2140
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 6.832934745473181e-4
allele num: 5854
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

FS
type: SiteQuality
SIO_000300: 4.014e0

VQSLOD
type: SiteQuality
SIO_000300: 3.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

DP
type: SiteQuality
SIO_000300: 9.03477e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-2

QD
type: SiteQuality
SIO_000300: 1.536e1

GenotypeQuality
all individuals: 439
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28794
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
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variant carriers: 0

GenotypeQuality
all individuals: 636
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GenotypeQuality
all individuals: 1770
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variant carriers: 0

GenotypeQuality
all individuals: 432
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GenotypeQuality
all individuals: 2492
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variant carriers: 0

GenotypeQuality
all individuals: 1314
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 241
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variant carriers: 0

GenotypeQuality
all individuals: 2454
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5940
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.898253606681853e-4
allele num: 5268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4316
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.936e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

FS
type: SiteQuality
SIO_000300: 7.403e0

QD
type: SiteQuality
SIO_000300: 1.294e1

MQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

DP
type: SiteQuality
SIO_000300: 9.14269e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 240
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16213
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1852
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 344
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GenotypeQuality
all individuals: 293
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GenotypeQuality
all individuals: 771
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variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5748
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5014
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.665278934221482e-4
allele num: 12010
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.029568589432865e-5
allele num: 33008
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.949e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

QD
type: SiteQuality
SIO_000300: 8.32e0

DP
type: SiteQuality
SIO_000300: 9.58666e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 742
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2710
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5014
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12010
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5748
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.581277672359266e-4
allele num: 6324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

DP
type: SiteQuality
SIO_000300: 9.58666e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.949e0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

QD
type: SiteQuality
SIO_000300: 8.32e0

GenotypeQuality
all individuals: 953
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variant carriers: 0

GenotypeQuality
all individuals: 582
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1890
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GenotypeQuality
all individuals: 711
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GenotypeQuality
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GenotypeQuality
all individuals: 1850
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1099
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12696
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6966
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.622849724115547e-4
allele num: 6162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3528
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.03069e6

VQSLOD
type: SiteQuality
SIO_000300: 7.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.137e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

FS
type: SiteQuality
SIO_000300: 3.279e0

QD
type: SiteQuality
SIO_000300: 9.32e0

MQRankSum
type: SiteQuality
SIO_000300: -5.45e-1

GenotypeQuality
all individuals: 2693
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1855
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 729
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6264
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 2.511553144464537e-4
allele num: 39816
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.942e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.189e1

FS
type: SiteQuality
SIO_000300: 5.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.94e0

DP
type: SiteQuality
SIO_000300: 1.036956e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

GenotypeQuality
all individuals: 106
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variant carriers: 0

GenotypeQuality
all individuals: 573
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GenotypeQuality
all individuals: 22313
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GenotypeQuality
all individuals: 2059
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GenotypeQuality
all individuals: 1847
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GenotypeQuality
all individuals: 540
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GenotypeQuality
all individuals: 242
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GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1095
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.550387596899225e-4
allele num: 6450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3696
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40738
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12822
num of homozygotes: 0

FS
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.546e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

DP
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SIO_000300: 1.048366e6

InbreedingCoeff
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SIO_000300: -4.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

VQSLOD
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SIO_000300: 2.08e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

QD
type: SiteQuality
SIO_000300: 1.078e1

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: 2.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7530
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 7322
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13294
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 4.37598459653422e-5
allele num: 45704
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 656
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4182
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.351e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

VQSLOD
type: SiteQuality
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QD
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SIO_000300: 1.165e1

MQRankSum
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SIO_000300: -3.96e-1

DP
type: SiteQuality
SIO_000300: 1.10889e6

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
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allele frequency: 0.0e0
allele num: 7682
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 7012
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South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 672
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4422
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 4.194806829145518e-5
allele num: 47678
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 7704
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.136455e6

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

MQRankSum
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SIO_000300: -3.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.598e0

VQSLOD
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SIO_000300: 5.2e-2

MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 1.256e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.87e-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: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4498
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.066798941798942e-5
allele num: 48384
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7058
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7772
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.26e-2

DP
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SIO_000300: 1.146864e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: -1.036e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

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 (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8038
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.93475989629687e-5
allele num: 51686
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13876
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

FS
type: SiteQuality
SIO_000300: 2.072e0

VQSLOD
type: SiteQuality
SIO_000300: 1.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.98e0

DP
type: SiteQuality
SIO_000300: 1.191413e6

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.223990208078335e-4
allele num: 8170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52910
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7478
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14000
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.23e-1

DP
type: SiteQuality
SIO_000300: 1.2132e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.398e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.459e1

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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Other
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allele count: 0
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num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.850275691077971e-5
allele num: 54046
num of homozygotes: 0

South Asian
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num of homozygotes: 0

QD
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VQSLOD
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MQRankSum
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DP
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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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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variant carriers: 4

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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allele frequency: 0.0e0
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Latino
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 7.151029748283753e-5
allele num: 55936
num of homozygotes: 0

VQSLOD
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DP
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MQ
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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QD
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FS
type: SiteQuality
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InbreedingCoeff
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 56788
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Other
type: Population
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num of homozygotes: 0

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

DP
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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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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European (Finnish)
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allele num: 5356
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 56788
num of homozygotes: 0

Latino
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East Asian
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allele frequency: 1.265822784810127e-4
allele num: 7900
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South Asian
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African
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Other
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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DP
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MQ
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.713854802221156e-5
allele num: 58348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5526
num of homozygotes: 0

Latino
type: Population
allele count: 32
allele frequency: 3.284072249589491e-3
allele num: 9744
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8776
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.278772378516624e-3
allele num: 782
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.322508e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

QD
type: SiteQuality
SIO_000300: 1.214e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

FS
type: SiteQuality
SIO_000300: 1.277e0

GenotypeQuality
all individuals: 35427
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 967
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14738
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.27894257064722e-4
allele num: 8776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

QD
type: SiteQuality
SIO_000300: 1.214e1

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 1.277e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.322508e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3279
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variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15056
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.213297743266198e-4
allele num: 8242
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9052
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.655245472903632e-5
allele num: 60414
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.53e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.367947e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.0e-1

FS
type: SiteQuality
SIO_000300: 2.699e0

QD
type: SiteQuality
SIO_000300: 1.13e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.03e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 9.75e1
variant carriers: 21

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5936
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 3.082414016872161e-4
allele num: 61640
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.906214258482653e-4
allele num: 10492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15296
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.396477e6

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

QD
type: SiteQuality
SIO_000300: 1.112e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.409e0

FS
type: SiteQuality
SIO_000300: 2.524e0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

GenotypeQuality
all individuals: 867
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 44031
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GenotypeQuality
all individuals: 3510
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9362
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.454111268878275e-5
allele num: 15494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10694
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.917e1

FS
type: SiteQuality
SIO_000300: 1.184e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.22e-1

QD
type: SiteQuality
SIO_000300: 1.14e1

DP
type: SiteQuality
SIO_000300: 1.416015e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.58e-1

GenotypeQuality
all individuals: 863
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 255
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GenotypeQuality
all individuals: 3515
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44376
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1850
bin: 9.75e1
variant carriers: 9

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6068
num of homozygotes: 0

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

East Asian
type: Population
allele count: 9
allele frequency: 1.068629779149846e-3
allele num: 8422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10734
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.287e0

VQSLOD
type: SiteQuality
SIO_000300: 2.85e0

FS
type: SiteQuality
SIO_000300: 1.133e0

DP
type: SiteQuality
SIO_000300: 1.420497e6

QD
type: SiteQuality
SIO_000300: 1.057e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

GenotypeQuality
all individuals: 481
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
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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
all individuals: 252
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GenotypeQuality
all individuals: 729
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 3.181336161187699e-4
allele num: 9430
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.173708920187793e-3
allele num: 852
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.287001287001287e-4
allele num: 15540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 83
allele frequency: 1.323130878367607e-3
allele num: 62730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 8.358098068350668e-4
allele num: 10768
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

QD
type: SiteQuality
SIO_000300: 1.161e1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.021e0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-2

DP
type: SiteQuality
SIO_000300: 1.424665e6

GenotypeQuality
all individuals: 135
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 462
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62964
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.922337562475971e-4
allele num: 15606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

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

African
type: Population
allele count: 15
allele frequency: 1.584283903675539e-3
allele num: 9468
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

DP
type: SiteQuality
SIO_000300: 1.429534e6

QD
type: SiteQuality
SIO_000300: 1.353e1

FS
type: SiteQuality
SIO_000300: 3.189e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 420
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GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 358
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GenotypeQuality
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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: 176
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11002
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.566514192618585e-5
allele num: 63836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.602e0

FS
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.453026e6

GenotypeQuality
all individuals: 423
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1841
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 198
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11098
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.233636703652911e-5
allele num: 64168
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 8.880000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.442e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

FS
type: SiteQuality
SIO_000300: 3.679e0

DP
type: SiteQuality
SIO_000300: 1.463757e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.75e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555839064007219e-5
allele num: 64274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 1.467884e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.135e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQRankSum
type: SiteQuality
SIO_000300: 9.15e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeQuality
all individuals: 48258
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1838
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16040
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549090683768628e-5
allele num: 64554
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

QD
type: SiteQuality
SIO_000300: 1.873e1

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 1.477e0

DP
type: SiteQuality
SIO_000300: 1.477371e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1837
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 301
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16046
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547891771407343e-5
allele num: 64604
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11186
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.435e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 1.478146e6

MQ
type: SiteQuality
SIO_000300: 5.721e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 3.65e0

FS
type: SiteQuality
SIO_000300: 4.404e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.002e0

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-1

GenotypeQuality
all individuals: 2326
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 900
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variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 755
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 289
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variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1847
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 409
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.643244079863798e-5
allele num: 64610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9920
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16038
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11182
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

DP
type: SiteQuality
SIO_000300: 1.478663e6

FS
type: SiteQuality
SIO_000300: 2.499e0

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47953
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variant carriers: 0

GenotypeQuality
all individuals: 320
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variant carriers: 0

GenotypeQuality
all individuals: 900
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GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 329
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variant carriers: 0

GenotypeQuality
all individuals: 244
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GenotypeQuality
all individuals: 755
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 1847
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 386
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547748026621266e-5
allele num: 64610
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.133786848072562e-3
allele num: 882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.78858880343409e-4
allele num: 11182
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16038
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.497318722312894e-4
allele num: 8578
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.008064516129032e-4
allele num: 9920
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

FS
type: SiteQuality
SIO_000300: 2.499e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-2

DP
type: SiteQuality
SIO_000300: 1.478663e6

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

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 275
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GenotypeQuality
all individuals: 1840
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variant carriers: 4

GenotypeQuality
all individuals: 320
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GenotypeQuality
all individuals: 72
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GenotypeQuality
all individuals: 176
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 48303
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166044776119403e-4
allele num: 8576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11186
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.09377223648795e-5
allele num: 64646
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.228977201943441e-5
allele num: 16054
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.480228e6

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1845
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 887
bin: 7.25e1
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GenotypeQuality
all individuals: 42
bin: 1.75e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 3666
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GenotypeQuality
all individuals: 78
bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 48302
bin: 6.25e1
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GenotypeQuality
all individuals: 415
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GenotypeQuality
all individuals: 345
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9918
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
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: 11192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.238083446824316e-4
allele num: 64616
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.479511e6

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

FS
type: SiteQuality
SIO_000300: 5.121e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: -1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

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

GenotypeQuality
all individuals: 173
bin: 8.75e1
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GenotypeQuality
all individuals: 881
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
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GenotypeQuality
all individuals: 246
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GenotypeQuality
all individuals: 737
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GenotypeQuality
all individuals: 1844
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 344
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GenotypeQuality
all individuals: 48520
bin: 6.25e1
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GenotypeQuality
all individuals: 157
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GenotypeQuality
all individuals: 41
bin: 1.75e1
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GenotypeQuality
all individuals: 218
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547316952404531e-5
allele num: 64628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16084
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11190
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.007658202337767e-4
allele num: 9924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.479967e6

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 4.182e0

QD
type: SiteQuality
SIO_000300: 8.539999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

GenotypeQuality
all individuals: 124
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3671
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 5.25e1
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GenotypeQuality
all individuals: 309
bin: 3.25e1
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GenotypeQuality
all individuals: 223
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GenotypeQuality
all individuals: 157
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GenotypeQuality
all individuals: 881
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GenotypeQuality
all individuals: 2384
bin: 2.25e1
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GenotypeQuality
all individuals: 737
bin: 7.75e1
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GenotypeQuality
all individuals: 406
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GenotypeQuality
all individuals: 218
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48520
bin: 6.25e1
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GenotypeQuality
all individuals: 173
bin: 8.75e1
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GenotypeQuality
all individuals: 246
bin: 9.25e1
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GenotypeQuality
all individuals: 1844
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.641950857213592e-5
allele num: 64628
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16084
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.182e0

QD
type: SiteQuality
SIO_000300: 8.539999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

DP
type: SiteQuality
SIO_000300: 1.479967e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.62e-1

GenotypeQuality
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bin: 7.5e0
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15940
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11084
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.17426021606388e-4
allele num: 8516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63994
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.381e0

BaseQRankSum
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SIO_000300: 2.43e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.348e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8504
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.043226623259179e-5
allele num: 11058
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -5.628e-1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-1

FS
type: SiteQuality
SIO_000300: 8.625e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-2

DP
type: SiteQuality
SIO_000300: 1.4507e6

MQRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.272e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.32351081320349e-5
allele num: 15814
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10952
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.547e0

QD
type: SiteQuality
SIO_000300: 1.14e1

VQSLOD
type: SiteQuality
SIO_000300: -1.972e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.429813e6

MQRankSum
type: SiteQuality
SIO_000300: -2.371e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.66e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 240
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9594
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584987003106575e-5
allele num: 63092
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.358087487283825e-5
allele num: 15728
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.165e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.414e0

QD
type: SiteQuality
SIO_000300: 1.342e1

VQSLOD
type: SiteQuality
SIO_000300: 3.23e-1

DP
type: SiteQuality
SIO_000300: 1.415199e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.15e-1

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10746
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.053962900505902e-4
allele num: 9488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15548
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62298
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
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SIO_000300: 1.37324e6

FS
type: SiteQuality
SIO_000300: 4.045e0

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-2

MQ
type: SiteQuality
SIO_000300: 5.771e1

QD
type: SiteQuality
SIO_000300: 1.078e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 10
allele frequency: 1.605187967510995e-4
allele num: 62298
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.611343860779891e-4
allele num: 6206
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.28633907898122e-4
allele num: 15548
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 9.305788200260562e-5
allele num: 10746
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9488
num of homozygotes: 0

Other
type: Population
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allele num: 844
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

BaseQRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: 5.3e-2

InbreedingCoeff
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SIO_000300: 1.1e-3

DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
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SIO_000300: 5.771e1

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-1

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
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num of homozygotes: 0

South Asian
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allele frequency: 1.944516463572725e-4
allele num: 15428
num of homozygotes: 0

Latino
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allele num: 10648
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East Asian
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Other
type: Population
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European (Non-Finnish)
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allele count: 17
allele frequency: 2.747696783578471e-4
allele num: 61870
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
type: SiteQuality
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BaseQRankSum
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QD
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DP
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SIO_000300: 1.340219e6

FS
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

East Asian
type: Population
allele count: 0
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num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.761904761904762e-3
allele num: 840
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Latino
type: Population
allele count: 9
allele frequency: 8.498583569405099e-4
allele num: 10590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 36
allele frequency: 5.841121495327102e-4
allele num: 61632
num of homozygotes: 0

African
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allele count: 236
allele frequency: 2.521906390254328e-2
allele num: 9358
num of homozygotes: 4

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15378
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.09e-2

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.1e-1

DP
type: SiteQuality
SIO_000300: 1.316437e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.39e-1

QD
type: SiteQuality
SIO_000300: 1.393e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e-1

GenotypeQuality
all individuals: 1821
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 335
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1530
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34548
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3141
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2735
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10678
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9286
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.46611132146914e-5
allele num: 10564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15360
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

QD
type: SiteQuality
SIO_000300: 1.11e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.717000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 1.30308e6

VQSLOD
type: SiteQuality
SIO_000300: 5.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.735e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

GenotypeQuality
all individuals: 330
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3251
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31197
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11689
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 9.75e1
variant carriers: 4

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9244
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15286
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.45398773006135e-4
allele num: 8150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.260302556077204e-5
allele num: 61344
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

FS
type: SiteQuality
SIO_000300: 5.382e0

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 1.270805e6

QD
type: SiteQuality
SIO_000300: 1.207e1

GenotypeQuality
all individuals: 6293
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23424
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3578
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4485
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13627
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.646144729044577e-5
allele num: 60748
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8070
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 1.18514e6

MQRankSum
type: SiteQuality
SIO_000300: -8.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

VQSLOD
type: SiteQuality
SIO_000300: 4.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.215e0

QD
type: SiteQuality
SIO_000300: 1.317e1

GenotypeQuality
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18851
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4578
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13982
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1066
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 471
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6038
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7970
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.657440249279014e-5
allele num: 60334
num of homozygotes: 0