18-6244447-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244447
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244447
    reference: chr 18
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.324+36T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.324+36T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.324+36T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.324+36T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.324+36T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.324+36T>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7504
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3600
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29471
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4165
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3767
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9982
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

18-6244451-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244451
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244451
    reference: chr 18
allele count: 550
allele frequency: 4.55509176439409e-3
allele num: 120744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.324+32T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.324+32T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.324+32T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.324+32T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.324+32T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.324+32T>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 8.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 8.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 6.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 6910
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 9.75e1
  variant carriers: 279
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 7465
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 7351
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 5.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 5.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 2.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3582
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10248
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4227
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3755
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 7.25e1
  variant carriers: 1
num of homozygotes: 12
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

18-6244452-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244452
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244452
    reference: chr 18
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.324+31T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.324+31T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.324+31T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.324+31T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.324+31T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.324+31T>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3617
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3721
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10423
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-6244475-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244475
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244475
    reference: chr 18
allele count: 7
allele frequency: 5.778056591937135e-5
allele num: 121148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.324+8G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.324+8G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.324+8G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.324+8G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.324+8G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.324+8G>A
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6819
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3724
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11372
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1969
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
hgvs: c.324+8G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

18-6244486-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244486
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244486
    reference: chr 18
allele count: 4
allele frequency: 3.298805832288711e-5
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.321G>A
  hgvsp: ENST00000400104.3:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.321G>A
  hgvsp: ENST00000284898.6:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.321G>A
  hgvsp: ENST00000583809.1:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.321G>A
  hgvsp: ENST00000400105.2:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.321G>A
  hgvsp: ENST00000317931.7:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.321G>A
  hgvsp: ENST00000583054.1:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29306
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4391
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala107Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

18-6244487-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244487
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244487
    reference: chr 18
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.320C>T
  hgvsp: ENSP00000463600.1:p.Ala107Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.320C>T
  hgvsp: ENSP00000284898.6:p.Ala107Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.320C>T
  hgvsp: ENSP00000382975.3:p.Ala107Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.320C>T
  hgvsp: ENSP00000462090.1:p.Ala107Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.320C>T
  hgvsp: ENSP00000318543.7:p.Ala107Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.320C>T
  hgvsp: ENSP00000382976.2:p.Ala107Val
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29304
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3779
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4397
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala107Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/18-6244492-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244492
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244492
    reference: chr 18
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.315T>G
  hgvsp: ENST00000583054.1:c.315T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.315T>G
  hgvsp: ENST00000583809.1:c.315T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.315T>G
  hgvsp: ENST00000284898.6:c.315T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.315T>G
  hgvsp: ENST00000317931.7:c.315T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.315T>G
  hgvsp: ENST00000400105.2:c.315T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.315T>G
  hgvsp: ENST00000400104.3:c.315T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4405
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3724
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3779
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11748
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser105Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

18-6244492-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244492
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244492
    reference: chr 18
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.315T>C
  hgvsp: ENST00000583054.1:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.315T>C
  hgvsp: ENST00000583809.1:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.315T>C
  hgvsp: ENST00000317931.7:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.315T>C
  hgvsp: ENST00000400105.2:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.315T>C
  hgvsp: ENST00000284898.6:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.315T>C
  hgvsp: ENST00000400104.3:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4405
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29303
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3724
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser105Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

18-6244498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244498
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244498
    reference: chr 18
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.309G>A
  hgvsp: ENST00000583809.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.309G>A
  hgvsp: ENST00000400104.3:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.309G>A
  hgvsp: ENST00000583054.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.309G>A
  hgvsp: ENST00000317931.7:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.309G>A
  hgvsp: ENST00000400105.2:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.309G>A
  hgvsp: ENST00000284898.6:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3723
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11774
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val103Val
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/18-6244503-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244503
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244503
    reference: chr 18
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.304T>G
  hgvsp: ENSP00000382976.2:p.Cys102Gly
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.304T>G
  hgvsp: ENSP00000284898.6:p.Cys102Gly
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.304T>G
  hgvsp: ENSP00000462090.1:p.Cys102Gly
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.304T>G
  hgvsp: ENSP00000463600.1:p.Cys102Gly
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.304T>G
  hgvsp: ENSP00000318543.7:p.Cys102Gly
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.304T>G
  hgvsp: ENSP00000382975.3:p.Cys102Gly
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3617
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3778
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Cys102Gly
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

18-6244503-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244503
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244503
    reference: chr 18
allele count: 4
allele frequency: 3.297065611605671e-5
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.304T>A
  hgvsp: ENSP00000463600.1:p.Cys102Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.304T>A
  hgvsp: ENSP00000284898.6:p.Cys102Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.304T>A
  hgvsp: ENSP00000382976.2:p.Cys102Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.304T>A
  hgvsp: ENSP00000462090.1:p.Cys102Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.304T>A
  hgvsp: ENSP00000382975.3:p.Cys102Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.304T>A
  hgvsp: ENSP00000318543.7:p.Cys102Ser
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4402
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3778
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys102Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

18-6244507-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244507
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244507
    reference: chr 18
allele count: 99
allele frequency: 8.159968349213675e-4
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.300A>G
  hgvsp: ENST00000400105.2:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.300A>G
  hgvsp: ENST00000317931.7:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.300A>G
  hgvsp: ENST00000284898.6:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.300A>G
  hgvsp: ENST00000583809.1:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.300A>G
  hgvsp: ENST00000400104.3:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.300A>G
  hgvsp: ENST00000583054.1:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6922
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 9.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3777
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3720
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3612
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val100Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

18-6244510-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244510
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244510
    reference: chr 18
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.297G>A
  hgvsp: ENST00000400104.3:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.297G>A
  hgvsp: ENST00000583809.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.297G>A
  hgvsp: ENST00000583054.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.297G>A
  hgvsp: ENST00000317931.7:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.297G>A
  hgvsp: ENST00000284898.6:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.297G>A
  hgvsp: ENST00000400105.2:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3786
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4402
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser99Ser
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

18-6244516-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244516
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244516
    reference: chr 18
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.291T>C
  hgvsp: ENST00000583054.1:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.291T>C
  hgvsp: ENST00000400104.3:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.291T>C
  hgvsp: ENST00000583809.1:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.291T>C
  hgvsp: ENST00000317931.7:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.291T>C
  hgvsp: ENST00000284898.6:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.291T>C
  hgvsp: ENST00000400105.2:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11843
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4407
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His97His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

18-6244520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244520
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244520
    reference: chr 18
allele count: 3
allele frequency: 2.472432378974435e-5
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.287G>A
  hgvsp: ENSP00000463600.1:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.287G>A
  hgvsp: ENSP00000382975.3:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.287G>A
  hgvsp: ENSP00000318543.7:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.287G>A
  hgvsp: ENSP00000284898.6:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.287G>A
  hgvsp: ENSP00000462090.1:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.287G>A
  hgvsp: ENSP00000382976.2:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11835
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3728
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg96Gln
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

18-6244521-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244521
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244521
    reference: chr 18
allele count: 7
allele frequency: 5.769103975736797e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.286C>T
  hgvsp: ENSP00000382976.2:p.Arg96Ter
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.286C>T
  hgvsp: ENSP00000284898.6:p.Arg96Ter
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.286C>T
  hgvsp: ENSP00000318543.7:p.Arg96Ter
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.286C>T
  hgvsp: ENSP00000462090.1:p.Arg96Ter
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.286C>T
  hgvsp: ENSP00000382975.3:p.Arg96Ter
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.286C>T
  hgvsp: ENSP00000463600.1:p.Arg96Ter
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3726
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg96Ter
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS

http://identifiers.org/exac.variant/18-6244536-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244536
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244536
    reference: chr 18
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.271G>T
  hgvsp: ENSP00000382975.3:p.Glu91Ter
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.271G>T
  hgvsp: ENSP00000284898.6:p.Glu91Ter
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.271G>T
  hgvsp: ENSP00000462090.1:p.Glu91Ter
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.271G>T
  hgvsp: ENSP00000463600.1:p.Glu91Ter
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.271G>T
  hgvsp: ENSP00000382976.2:p.Glu91Ter
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.271G>T
  hgvsp: ENSP00000318543.7:p.Glu91Ter
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3788
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3727
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11815
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu91Ter
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

18-6244540-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244540
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244540
    reference: chr 18
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.267A>C
  hgvsp: ENSP00000382976.2:p.Arg89Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.267A>C
  hgvsp: ENSP00000463600.1:p.Arg89Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.267A>C
  hgvsp: ENSP00000382975.3:p.Arg89Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.267A>C
  hgvsp: ENSP00000318543.7:p.Arg89Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.267A>C
  hgvsp: ENSP00000462090.1:p.Arg89Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.267A>C
  hgvsp: ENSP00000284898.6:p.Arg89Ser
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3725
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3788
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11822
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg89Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/18-6244544-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244544
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244544
    reference: chr 18
allele count: 2
allele frequency: 1.648342591524222e-5
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.263T>G
  hgvsp: ENSP00000462090.1:p.Met88Arg
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.263T>G
  hgvsp: ENSP00000382975.3:p.Met88Arg
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.263T>G
  hgvsp: ENSP00000463600.1:p.Met88Arg
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.263T>G
  hgvsp: ENSP00000284898.6:p.Met88Arg
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.263T>G
  hgvsp: ENSP00000318543.7:p.Met88Arg
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.263T>G
  hgvsp: ENSP00000382976.2:p.Met88Arg
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29260
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11818
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3619
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met88Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/18-6244547-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244547
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244547
    reference: chr 18
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.260G>T
  hgvsp: ENSP00000284898.6:p.Gly87Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.260G>T
  hgvsp: ENSP00000382976.2:p.Gly87Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.260G>T
  hgvsp: ENSP00000463600.1:p.Gly87Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.260G>T
  hgvsp: ENSP00000318543.7:p.Gly87Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.260G>T
  hgvsp: ENSP00000382975.3:p.Gly87Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.260G>T
  hgvsp: ENSP00000462090.1:p.Gly87Val
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3724
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29260
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1978
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11816
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly87Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

18-6244566-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244566
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244566
    reference: chr 18
allele count: 14
allele frequency: 1.154334526145677e-4
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.241G>A
  hgvsp: ENSP00000284898.6:p.Glu81Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.241G>A
  hgvsp: ENSP00000382975.3:p.Glu81Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.241G>A
  hgvsp: ENSP00000318543.7:p.Glu81Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.241G>A
  hgvsp: ENSP00000462090.1:p.Glu81Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.241G>A
  hgvsp: ENSP00000463600.1:p.Glu81Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.241G>A
  hgvsp: ENSP00000382976.2:p.Glu81Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.241G>A
  hgvsp: ENST00000581231.1:c.241G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1997
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29259
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu81Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-6244566-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244566
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244566
    reference: chr 18
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.241G>C
  hgvsp: ENSP00000318543.7:p.Glu81Gln
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.241G>C
  hgvsp: ENSP00000382975.3:p.Glu81Gln
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.241G>C
  hgvsp: ENST00000581231.1:c.241G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.241G>C
  hgvsp: ENSP00000463600.1:p.Glu81Gln
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.241G>C
  hgvsp: ENSP00000462090.1:p.Glu81Gln
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.241G>C
  hgvsp: ENSP00000382976.2:p.Glu81Gln
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.241G>C
  hgvsp: ENSP00000284898.6:p.Glu81Gln
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3726
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1997
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4402
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu81Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

18-6244569-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244569
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244569
    reference: chr 18
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.238C>T
  hgvsp: ENSP00000462295.1:p.His80Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.238C>T
  hgvsp: ENSP00000382975.3:p.His80Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.238C>T
  hgvsp: ENSP00000462090.1:p.His80Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.238C>T
  hgvsp: ENSP00000318543.7:p.His80Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.238C>T
  hgvsp: ENSP00000382976.2:p.His80Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.238C>T
  hgvsp: ENSP00000463600.1:p.His80Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.238C>T
  hgvsp: ENSP00000284898.6:p.His80Tyr
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4400
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11730
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His80Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

18-6244580-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244580
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244580
    reference: chr 18
allele count: 2
allele frequency: 1.650110557407346e-5
allele num: 121204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.227C>T
  hgvsp: ENSP00000462295.1:p.Ser76Phe
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.227C>T
  hgvsp: ENSP00000462090.1:p.Ser76Phe
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.227C>T
  hgvsp: ENSP00000284898.6:p.Ser76Phe
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.227C>T
  hgvsp: ENSP00000382976.2:p.Ser76Phe
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.227C>T
  hgvsp: ENSP00000318543.7:p.Ser76Phe
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.227C>T
  hgvsp: ENSP00000382975.3:p.Ser76Phe
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.227C>T
  hgvsp: ENSP00000463600.1:p.Ser76Phe
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29252
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3723
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser76Phe
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

18-6244580-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244580
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244580
    reference: chr 18
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.227C>A
  hgvsp: ENSP00000382976.2:p.Ser76Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.227C>A
  hgvsp: ENSP00000463600.1:p.Ser76Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.227C>A
  hgvsp: ENSP00000462090.1:p.Ser76Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.227C>A
  hgvsp: ENSP00000284898.6:p.Ser76Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.227C>A
  hgvsp: ENSP00000318543.7:p.Ser76Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.227C>A
  hgvsp: ENSP00000382975.3:p.Ser76Tyr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.227C>A
  hgvsp: ENSP00000462295.1:p.Ser76Tyr
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3608
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11602
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4384
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser76Tyr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

18-6244585-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244585
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244585
    reference: chr 18
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.222T>C
  hgvsp: ENST00000284898.6:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.222T>C
  hgvsp: ENST00000581231.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.222T>C
  hgvsp: ENST00000583054.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.222T>C
  hgvsp: ENST00000583809.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.222T>C
  hgvsp: ENST00000400105.2:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.222T>C
  hgvsp: ENST00000400104.3:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.222T>C
  hgvsp: ENST00000317931.7:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3607
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3724
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11438
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
hgvs: c.222T>C
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

18-6244587-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244587
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244587
    reference: chr 18
allele count: 3
allele frequency: 2.476637057094739e-5
allele num: 121132
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.220G>C
  hgvsp: ENSP00000462090.1:p.Asp74His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.220G>C
  hgvsp: ENSP00000284898.6:p.Asp74His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.220G>C
  hgvsp: ENSP00000382975.3:p.Asp74His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.220G>C
  hgvsp: ENSP00000318543.7:p.Asp74His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.220G>C
  hgvsp: ENSP00000462295.1:p.Asp74His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.220G>C
  hgvsp: ENSP00000382976.2:p.Asp74His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.220G>C
  hgvsp: ENSP00000463600.1:p.Asp74His
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1994
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11446
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp74His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

18-6244601-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244601
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244601
    reference: chr 18
allele count: 4
allele frequency: 3.306932985003059e-5
allele num: 120958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.220-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.220-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.220-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.220-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.220-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.220-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.220-14G>A
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3586
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1936
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1992
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

18-6244602-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244602
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244602
    reference: chr 18
allele count: 2
allele frequency: 1.653603201375798e-5
allele num: 120948
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.220-15C>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.220-15C>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.220-15C>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.220-15C>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.220-15C>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.220-15C>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.220-15C>T
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7407
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3588
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3787
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10746
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

18-6244608-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244608
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244608
    reference: chr 18
allele count: 2
allele frequency: 1.654807214959457e-5
allele num: 120860
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.220-21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.220-21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.220-21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.220-21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.220-21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.220-21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.220-21T>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3580
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29249
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10086
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1987
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP

18-6244615-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244615
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244615
    reference: chr 18
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.220-28G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.220-28G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.220-28G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.220-28G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.220-28G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.220-28G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.220-28G>A
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4132
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3711
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

18-6244629-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244629
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244629
    reference: chr 18
allele count: 1
allele frequency: 8.298066550493736e-6
allele num: 120510
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.220-42A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.220-42A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.220-42A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.220-42A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.220-42A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.220-42A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.220-42A>G
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6905
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3786
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3781
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

18-6244630-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244630
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244630
    reference: chr 18
allele count: 1
allele frequency: 8.307993951780402e-6
allele num: 120366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.220-43G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.220-43G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.220-43G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.220-43G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.220-43G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.220-43G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.220-43G>A
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6920
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3691
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29241
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1339
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6667
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

18-6244639-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6244639
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6244639
    reference: chr 18
allele count: 1
allele frequency: 8.343345347750633e-6
allele num: 119856
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.220-52T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.220-52T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.220-52T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.220-52T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.220-52T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.220-52T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.220-52T>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29238
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1027
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

18-6263901-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263901
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263901
    reference: chr 18
allele count: 6
allele frequency: 5.001166938952422e-5
allele num: 119972
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.219+45A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.219+45A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.219+45A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.219+45A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.219+45A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.219+45A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.219+45A>G
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14543
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9663
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7570
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2239
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4059
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1821
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1367
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

18-6263904-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263904
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263904
    reference: chr 18
allele count: 1
allele frequency: 8.335278231587371e-6
allele num: 119972
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.219+42C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.219+42C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.219+42C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.219+42C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.219+42C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.219+42C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.219+42C>G
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7536
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

18-6263908-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263908
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263908
    reference: chr 18
allele count: 1
allele frequency: 8.326256015719971e-6
allele num: 120102
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.219+38A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.219+38A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.219+38A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.219+38A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.219+38A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.219+38A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.219+38A>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15139
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3118
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7624
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2760
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS

18-6263910-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263910
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263910
    reference: chr 18
allele count: 1
allele frequency: 8.32251406504877e-6
allele num: 120156
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.219+36G>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.219+36G>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.219+36G>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.219+36G>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.219+36G>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.219+36G>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.219+36G>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4033
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2229
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum

18-6263912-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263912
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263912
    reference: chr 18
allele count: 1
allele frequency: 8.310065150910783e-6
allele num: 120336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.219+34A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.219+34A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.219+34A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.219+34A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.219+34A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.219+34A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.219+34A>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27764
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7721
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

18-6263925-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263925
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263925
    reference: chr 18
allele count: 3
allele frequency: 2.483772685123857e-5
allele num: 120784
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.219+21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.219+21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.219+21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.219+21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.219+21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.219+21T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.219+21T>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5662
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2235
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4040
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

18-6263927-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263927
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263927
    reference: chr 18
allele count: 1
allele frequency: 8.275953389830508e-6
allele num: 120832
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.219+19T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.219+19T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.219+19T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.219+19T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.219+19T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.219+19T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.219+19T>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3138
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

18-6263936-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263936
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263936
    reference: chr 18
allele count: 1
allele frequency: 8.259275166011431e-6
allele num: 121076
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.219+10T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.219+10T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.219+10T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.219+10T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.219+10T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.219+10T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.219+10T>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7848
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2232
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8419
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

18-6263938-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263938
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263938
    reference: chr 18
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.219+8A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.219+8A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.219+8A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.219+8A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.219+8A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.219+8A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.219+8A>G
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2232
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7857
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.25e1
  variant carriers: 0
hgvs: c.219+8A>G
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS

18-6263940-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263940
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263940
    reference: chr 18
allele count: 2
allele frequency: 1.650982334489021e-5
allele num: 121140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.219+6C>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.219+6C>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.219+6C>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.219+6C>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.219+6C>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.219+6C>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.219+6C>A
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.25e1
  variant carriers: 0
hgvs: c.219+6C>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-6263941-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263941
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263941
    reference: chr 18
allele count: 1
allele frequency: 8.253821519363466e-6
allele num: 121156
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.219+5G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.219+5G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.219+5G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.219+5G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.219+5G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.219+5G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.219+5G>A
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7859
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2231
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
hgvs: c.219+5G>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

18-6263966-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263966
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263966
    reference: chr 18
allele count: 3
allele frequency: 2.474267616785431e-5
allele num: 121248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.199C>T
  hgvsp: ENSP00000382976.2:p.Pro67Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.199C>T
  hgvsp: ENSP00000463600.1:p.Pro67Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.199C>T
  hgvsp: ENSP00000318543.7:p.Pro67Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.199C>T
  hgvsp: ENSP00000284898.6:p.Pro67Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.199C>T
  hgvsp: ENSP00000462090.1:p.Pro67Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.199C>T
  hgvsp: ENSP00000462295.1:p.Pro67Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.199C>T
  hgvsp: ENSP00000382975.3:p.Pro67Ser
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3128
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro67Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ

18-6263969-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263969
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263969
    reference: chr 18
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.196G>A
  hgvsp: ENSP00000382976.2:p.Ala66Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.196G>A
  hgvsp: ENSP00000463600.1:p.Ala66Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.196G>A
  hgvsp: ENSP00000462295.1:p.Ala66Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.196G>A
  hgvsp: ENSP00000284898.6:p.Ala66Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.196G>A
  hgvsp: ENSP00000318543.7:p.Ala66Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.196G>A
  hgvsp: ENSP00000382975.3:p.Ala66Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.196G>A
  hgvsp: ENSP00000462090.1:p.Ala66Thr
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2232
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30574
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7878
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala66Thr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

18-6263970-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263970
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263970
    reference: chr 18
allele count: 4
allele frequency: 3.299023489047242e-5
allele num: 121248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.195A>G
  hgvsp: ENST00000400105.2:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.195A>G
  hgvsp: ENST00000400104.3:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.195A>G
  hgvsp: ENST00000581231.1:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.195A>G
  hgvsp: ENST00000317931.7:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.195A>G
  hgvsp: ENST00000284898.6:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.195A>G
  hgvsp: ENST00000583054.1:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.195A>G
  hgvsp: ENST00000583809.1:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8420
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2802
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala65Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS

18-6263970-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263970
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263970
    reference: chr 18
allele count: 4
allele frequency: 3.299023489047242e-5
allele num: 121248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.195A>C
  hgvsp: ENST00000400104.3:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.195A>C
  hgvsp: ENST00000317931.7:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.195A>C
  hgvsp: ENST00000583054.1:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.195A>C
  hgvsp: ENST00000583809.1:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.195A>C
  hgvsp: ENST00000400105.2:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.195A>C
  hgvsp: ENST00000581231.1:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.195A>C
  hgvsp: ENST00000284898.6:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2232
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1362
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7880
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2802
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30586
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala65Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

18-6263973-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263973
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263973
    reference: chr 18
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.192C>T
  hgvsp: ENST00000583054.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.192C>T
  hgvsp: ENST00000583809.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.192C>T
  hgvsp: ENST00000581231.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.192C>T
  hgvsp: ENST00000284898.6:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.192C>T
  hgvsp: ENST00000400105.2:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.192C>T
  hgvsp: ENST00000317931.7:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.192C>T
  hgvsp: ENST00000400104.3:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30594
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2803
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val64Val
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

18-6263978-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263978
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263978
    reference: chr 18
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.187G>A
  hgvsp: ENSP00000382975.3:p.Ala63Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.187G>A
  hgvsp: ENSP00000462295.1:p.Ala63Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.187G>A
  hgvsp: ENSP00000318543.7:p.Ala63Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.187G>A
  hgvsp: ENSP00000284898.6:p.Ala63Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.187G>A
  hgvsp: ENSP00000462090.1:p.Ala63Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.187G>A
  hgvsp: ENSP00000382976.2:p.Ala63Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.187G>A
  hgvsp: ENSP00000463600.1:p.Ala63Thr
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2803
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30613
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala63Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/18-6263982-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263982
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263982
    reference: chr 18
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.183G>T
  hgvsp: ENSP00000463600.1:p.Gln61His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.183G>T
  hgvsp: ENSP00000462090.1:p.Gln61His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.183G>T
  hgvsp: ENSP00000382976.2:p.Gln61His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.183G>T
  hgvsp: ENSP00000318543.7:p.Gln61His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.183G>T
  hgvsp: ENSP00000462295.1:p.Gln61His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.183G>T
  hgvsp: ENSP00000284898.6:p.Gln61His
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.183G>T
  hgvsp: ENSP00000382975.3:p.Gln61His
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7891
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln61His
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

18-6263987-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263987
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263987
    reference: chr 18
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.178G>A
  hgvsp: ENSP00000284898.6:p.Glu60Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.178G>A
  hgvsp: ENSP00000382976.2:p.Glu60Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.178G>A
  hgvsp: ENSP00000463600.1:p.Glu60Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.178G>A
  hgvsp: ENSP00000462295.1:p.Glu60Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.178G>A
  hgvsp: ENSP00000318543.7:p.Glu60Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.178G>A
  hgvsp: ENSP00000382975.3:p.Glu60Lys
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.178G>A
  hgvsp: ENSP00000462090.1:p.Glu60Lys
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8414
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1362
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30594
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu60Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

18-6263993-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263993
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6263993
    reference: chr 18
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.172T>C
  hgvsp: ENST00000400105.2:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.172T>C
  hgvsp: ENST00000583054.1:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.172T>C
  hgvsp: ENST00000400104.3:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.172T>C
  hgvsp: ENST00000317931.7:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.172T>C
  hgvsp: ENST00000583809.1:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.172T>C
  hgvsp: ENST00000581231.1:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.172T>C
  hgvsp: ENST00000284898.6:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7893
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4047
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2231
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3132
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu58Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/18-6264008-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264008
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264008
    reference: chr 18
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.157T>G
  hgvsp: ENSP00000382975.3:p.Ser53Ala
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.157T>G
  hgvsp: ENSP00000463600.1:p.Ser53Ala
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.157T>G
  hgvsp: ENSP00000382976.2:p.Ser53Ala
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.157T>G
  hgvsp: ENSP00000462090.1:p.Ser53Ala
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.157T>G
  hgvsp: ENSP00000284898.6:p.Ser53Ala
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.157T>G
  hgvsp: ENSP00000318543.7:p.Ser53Ala
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.157T>G
  hgvsp: ENSP00000462295.1:p.Ser53Ala
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4044
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8413
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser53Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/18-6264014-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264014
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264014
    reference: chr 18
allele count: 2
allele frequency: 1.651200422707308e-5
allele num: 121124
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.151G>T
  hgvsp: ENSP00000284898.6:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.151G>T
  hgvsp: ENSP00000463600.1:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.151G>T
  hgvsp: ENSP00000318543.7:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.151G>T
  hgvsp: ENSP00000382975.3:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.151G>T
  hgvsp: ENSP00000462090.1:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.151G>T
  hgvsp: ENSP00000382976.2:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.151G>T
  hgvsp: ENSP00000462295.1:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30524
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala51Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

18-6264016-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264016
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264016
    reference: chr 18
allele count: 1
allele frequency: 8.257774694875225e-6
allele num: 121098
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.149G>A
  hgvsp: ENSP00000382976.2:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.149G>A
  hgvsp: ENSP00000462295.1:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.149G>A
  hgvsp: ENSP00000463600.1:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.149G>A
  hgvsp: ENSP00000318543.7:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.149G>A
  hgvsp: ENSP00000284898.6:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.149G>A
  hgvsp: ENSP00000462090.1:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.149G>A
  hgvsp: ENSP00000382975.3:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7858
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly50Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

18-6264026-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264026
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264026
    reference: chr 18
allele count: 1
allele frequency: 8.266785708380868e-6
allele num: 120966
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.139G>A
  hgvsp: ENSP00000318543.7:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.139G>A
  hgvsp: ENSP00000462295.1:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.139G>A
  hgvsp: ENSP00000382975.3:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.139G>A
  hgvsp: ENSP00000462090.1:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.139G>A
  hgvsp: ENSP00000382976.2:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.139G>A
  hgvsp: ENSP00000463600.1:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.139G>A
  hgvsp: ENSP00000284898.6:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3125
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2781
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4025
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala47Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

18-6264027-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264027
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264027
    reference: chr 18
allele count: 2
allele frequency: 1.653630545863443e-5
allele num: 120946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.138G>A
  hgvsp: ENST00000317931.7:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.138G>A
  hgvsp: ENST00000583809.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.138G>A
  hgvsp: ENST00000583054.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.138G>A
  hgvsp: ENST00000400104.3:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.138G>A
  hgvsp: ENST00000400105.2:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.138G>A
  hgvsp: ENST00000284898.6:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.138G>A
  hgvsp: ENST00000581231.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30406
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2779
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8412
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala46Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

18-6264028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264028
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264028
    reference: chr 18
allele count: 4
allele frequency: 3.307808080975142e-5
allele num: 120926
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.137C>T
  hgvsp: ENSP00000318543.7:p.Ala46Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.137C>T
  hgvsp: ENSP00000462090.1:p.Ala46Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.137C>T
  hgvsp: ENSP00000382975.3:p.Ala46Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.137C>T
  hgvsp: ENSP00000382976.2:p.Ala46Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.137C>T
  hgvsp: ENSP00000463600.1:p.Ala46Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.137C>T
  hgvsp: ENSP00000462295.1:p.Ala46Val
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.137C>T
  hgvsp: ENSP00000284898.6:p.Ala46Val
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3122
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8413
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala46Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/18-6264038-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264038
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264038
    reference: chr 18
allele count: 1
allele frequency: 8.281710670156027e-6
allele num: 120748
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.128-1G>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.128-1G>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.128-1G>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.128-1G>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.128-1G>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.128-1G>T
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.128-1G>T
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7812
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4020
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
hgvs: c.128-1G>T
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

18-6264051-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264051
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264051
    reference: chr 18
allele count: 1
allele frequency: 8.299306178003518e-6
allele num: 120492
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.128-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.128-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.128-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.128-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.128-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.128-14G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.128-14G>A
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16473
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4005
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 909
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

18-6264055-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264055
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264055
    reference: chr 18
allele count: 3
allele frequency: 2.491984117754556e-5
allele num: 120386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.128-18T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.128-18T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.128-18T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.128-18T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.128-18T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.128-18T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.128-18T>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10126
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8409
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7741
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

18-6264061-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264061
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264061
    reference: chr 18
allele count: 2
allele frequency: 1.663948883490299e-5
allele num: 120196
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.128-24A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.128-24A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.128-24A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.128-24A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.128-24A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.128-24A>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.128-24A>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10094
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7649
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3976
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

18-6264071-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264071
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264071
    reference: chr 18
allele count: 9
allele frequency: 7.505378854845973e-5
allele num: 119914
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.128-34A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.128-34A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.128-34A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.128-34A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.128-34A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.128-34A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.128-34A>G
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15402
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3089
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2209
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2184
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3945
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

18-6264077-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264077
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264077
    reference: chr 18
allele count: 8
allele frequency: 6.687397599224261e-5
allele num: 119628
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.128-40C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.128-40C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.128-40C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.128-40C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.128-40C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.128-40C>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.128-40C>G
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9459
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6101
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11857
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14179
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2449
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2349
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2208
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2645
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3919
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-6264080-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264080
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6264080
    reference: chr 18
allele count: 1
allele frequency: 8.375910880308233e-6
allele num: 119390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.128-43T>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.128-43T>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.128-43T>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.128-43T>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.128-43T>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.128-43T>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.128-43T>A
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1351
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2186
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17184
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

18-6301852-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6301852
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6301852
    reference: chr 18
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.127+50A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.127+50A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.127+50A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.127+50A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.127+50A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.127+50A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.127+50A>G
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

18-6301858-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6301858
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6301858
    reference: chr 18
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.127+44A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.127+44A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.127+44A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.127+44A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.127+44A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.127+44A>G
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.127+44A>G
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20962
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

18-6301872-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6301872
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6301872
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.127+30T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.127+30T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.127+30T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.127+30T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.127+30T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.127+30T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.127+30T>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57965
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

18-6301873-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6301873
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6301873
    reference: chr 18
allele count: 62
allele frequency: 5.106915752364008e-4
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.127+29G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.127+29G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.127+29G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.127+29G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.127+29G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.127+29G>A
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.127+29G>A
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20988
  bin: 9.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3712
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD

18-6301875-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6301875
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 6301875
    reference: chr 18
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382975
  ensembl transcript: ENST00000400104
  gene symbol: L3MBTL4
  hgvsc: ENST00000400104.3:c.127+27T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000284898
  ensembl transcript: ENST00000284898
  gene symbol: L3MBTL4
  hgvsc: ENST00000284898.6:c.127+27T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000318543
  ensembl transcript: ENST00000317931
  gene symbol: L3MBTL4
  hgvsc: ENST00000317931.7:c.127+27T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000382976
  ensembl transcript: ENST00000400105
  gene symbol: L3MBTL4
  hgvsc: ENST00000400105.2:c.127+27T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462295
  ensembl transcript: ENST00000581231
  gene symbol: L3MBTL4
  hgvsc: ENST00000581231.1:c.127+27T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000462090
  ensembl transcript: ENST00000583809
  gene symbol: L3MBTL4
  hgvsc: ENST00000583809.1:c.127+27T>C
  variant of: http://identifiers.org/hgnc/26677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154655
  ensembl protein: ENSP00000463600
  ensembl transcript: ENST00000583054
  gene symbol: L3MBTL4
  hgvsc: ENST00000583054.1:c.127+27T>C
  variant of: http://identifiers.org/hgnc/26677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4038
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20975
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57964
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 422
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1992
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.195786864931847e-5
allele num: 16140
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66448
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.15e-1

QD
type: SiteQuality
SIO_000300: 1.563e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.42e-1

DP
type: SiteQuality
SIO_000300: 2.814246e6

GenotypeQuality
all individuals: 1985
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3687
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29566
bin: 9.75e1
variant carriers: 537

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

Other
type: Population
allele count: 2
allele frequency: 2.217294900221729e-3
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 23
allele frequency: 1.989963661533137e-3
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 517
allele frequency: 4.979772683490657e-2
allele num: 10382
num of homozygotes: 12

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.203731567860367e-4
allele num: 66460
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.71e0

FS
type: SiteQuality
SIO_000300: 1.151e0

QD
type: SiteQuality
SIO_000300: 1.423e1

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-2

DP
type: SiteQuality
SIO_000300: 2.84124e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.13e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

GenotypeQuality
all individuals: 29310
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 131
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4277
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3775
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66466
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16186
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.097e0

MQRankSum
type: SiteQuality
SIO_000300: 2.91e0

MQ
type: SiteQuality
SIO_000300: 5.891e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.59e-1

QD
type: SiteQuality
SIO_000300: 1.691e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 2.814057e6

VQSLOD
type: SiteQuality
SIO_000300: -2.892e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.53e-1

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29313
bin: 9.75e1
variant carriers: 7

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

GenotypeQuality
all individuals: 4360
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501501501501501e-5
allele num: 66600
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 6
allele frequency: 3.654080389768575e-4
allele num: 16420
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.199e0

DP
type: SiteQuality
SIO_000300: 2.828572e6

QD
type: SiteQuality
SIO_000300: 1.388e1

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

GenotypeQuality
all individuals: 3778
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3610
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11622
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3724
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.923816852635629e-4
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001290554938624e-5
allele num: 66638
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.512e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.81e-1

QD
type: SiteQuality
SIO_000300: 1.336e1

DP
type: SiteQuality
SIO_000300: 2.831456e6

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3723
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11649
bin: 6.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.234e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.76e-1

DP
type: SiteQuality
SIO_000300: 2.8313e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.97e0

MQRankSum
type: SiteQuality
SIO_000300: -6.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-2

QD
type: SiteQuality
SIO_000300: 1.355e1

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29303
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1971
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3617
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.984e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.85e0

MQRankSum
type: SiteQuality
SIO_000300: -8.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

DP
type: SiteQuality
SIO_000300: 2.832245e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

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

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

GenotypeQuality
all individuals: 3779
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11748
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3617
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.984e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.85e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.832245e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

QD
type: SiteQuality
SIO_000300: 1.291e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

GenotypeQuality
all individuals: 4403
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29302
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1970
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3614
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3779
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.354e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 2.83228e6

VQSLOD
type: SiteQuality
SIO_000300: -2.097e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 1.783e0

QD
type: SiteQuality
SIO_000300: 9.6e0

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

GenotypeQuality
all individuals: 11802
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4402
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29302
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3724
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 7.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -6.54e-1

FS
type: SiteQuality
SIO_000300: 5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.231e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.45e-1

DP
type: SiteQuality
SIO_000300: 2.833147e6

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

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

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

GenotypeQuality
all individuals: 1999
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3617
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3724
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11802
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29302
bin: 9.75e1
variant carriers: 4

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

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

African
type: Population
allele count: 4
allele frequency: 3.847633705271258e-4
allele num: 10396
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.600000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.49e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 2.833147e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: -6.54e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.45e-1

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

GenotypeQuality
all individuals: 29321
bin: 9.75e1
variant carriers: 99

GenotypeQuality
all individuals: 4400
bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11795
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GenotypeQuality
all individuals: 1997
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variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.199760047990402e-4
allele num: 66680
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 86
allele frequency: 8.272412466333205e-3
allele num: 10396
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

DP
type: SiteQuality
SIO_000300: 2.842623e6

QD
type: SiteQuality
SIO_000300: 1.382e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 16504
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Other
type: Population
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

QD
type: SiteQuality
SIO_000300: 1.201e1

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

FS
type: SiteQuality
SIO_000300: 5.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.83162e6

MQ
type: SiteQuality
SIO_000300: 5.94e1

GenotypeQuality
all individuals: 3621
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3727
bin: 8.25e1
variant carriers: 0

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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.73e-1

QD
type: SiteQuality
SIO_000300: 1.007e1

FS
type: SiteQuality
SIO_000300: 1.0891e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.439e0

MQRankSum
type: SiteQuality
SIO_000300: 8.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.65e0

DP
type: SiteQuality
SIO_000300: 2.831765e6

MQ
type: SiteQuality
SIO_000300: 5.93e1

GenotypeQuality
all individuals: 29264
bin: 9.75e1
variant carriers: 3

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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GenotypeQuality
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GenotypeQuality
all individuals: 4410
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GenotypeQuality
all individuals: 1972
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.885170225043277e-4
allele num: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.832108e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 5.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e-1

QD
type: SiteQuality
SIO_000300: 1.425e1

GenotypeQuality
all individuals: 1999
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 4410
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 3788
bin: 9.25e1
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GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.497375918428549e-5
allele num: 66690
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

DP
type: SiteQuality
SIO_000300: 2.832626e6

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.96e0

QD
type: SiteQuality
SIO_000300: 1.238e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.22e-1

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

GenotypeQuality
all individuals: 4407
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
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GenotypeQuality
all individuals: 1999
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variant carriers: 0

GenotypeQuality
all individuals: 1977
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29262
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3619
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.36e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.31e-1

DP
type: SiteQuality
SIO_000300: 2.831686e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3619
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29262
bin: 9.75e1
variant carriers: 2

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

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

African
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allele frequency: 1.923816852635629e-4
allele num: 10396
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.26e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.831703e6

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
all individuals: 1979
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999040307101727e-5
allele num: 66688
num of homozygotes: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.74e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.807e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1

DP
type: SiteQuality
SIO_000300: 2.83186e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4404
bin: 6.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
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Other
type: Population
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South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.831606e6

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 3.281e0

VQSLOD
type: SiteQuality
SIO_000300: -7.169e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.797e0

QD
type: SiteQuality
SIO_000300: 9.56e0

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

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

GenotypeQuality
all individuals: 3614
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3789
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3726
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11760
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4402
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.350297065354378e-4
allele num: 66652
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.559721802237678e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.832055e6

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 2.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-2

QD
type: SiteQuality
SIO_000300: 1.281e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.732e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

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

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

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

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

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

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

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

GenotypeQuality
all individuals: 29259
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3789
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11760
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1971
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.832055e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.732e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

MQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-2

FS
type: SiteQuality
SIO_000300: 2.88e0

QD
type: SiteQuality
SIO_000300: 1.281e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 3791
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3613
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3725
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1970
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29252
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 5.22e-1

FS
type: SiteQuality
SIO_000300: 4.25e0

QD
type: SiteQuality
SIO_000300: 9.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

DP
type: SiteQuality
SIO_000300: 2.830413e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 7.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 1996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3789
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4384
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3608
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11602
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 7.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

QD
type: SiteQuality
SIO_000300: 1.271e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.866e0

FS
type: SiteQuality
SIO_000300: 6.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

DP
type: SiteQuality
SIO_000300: 2.829328e6

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3789
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3723
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29252
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1968
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 173
bin: 2.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.829328e6

MQ
type: SiteQuality
SIO_000300: 5.98e1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.866e0

FS
type: SiteQuality
SIO_000300: 6.57e-1

QD
type: SiteQuality
SIO_000300: 1.271e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.98e-1

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29252
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3788
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4372
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.43e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

FS
type: SiteQuality
SIO_000300: 6.675e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 1.109e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.75e-1

DP
type: SiteQuality
SIO_000300: 2.827435e6

VQSLOD
type: SiteQuality
SIO_000300: -4.03e-1

GenotypeQuality
all individuals: 4362
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3722
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3604
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3787
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29254
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.593809441466367e-4
allele num: 11566
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

DP
type: SiteQuality
SIO_000300: 2.827688e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

FS
type: SiteQuality
SIO_000300: 6.704e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.27e-2

QD
type: SiteQuality
SIO_000300: 1.362e1

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.92e-1

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 10757
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3786
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3715
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29253
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 641
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.225790634959549e-4
allele num: 16316
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502945773716484e-5
allele num: 66536
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.75e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.726e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.237e1

DP
type: SiteQuality
SIO_000300: 2.819883e6

GenotypeQuality
all individuals: 4243
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3714
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29250
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1934
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.313208420078649e-4
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.008e0

DP
type: SiteQuality
SIO_000300: 2.818493e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.242e0

VQSLOD
type: SiteQuality
SIO_000300: 9.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.169e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.346e1

GenotypeQuality
all individuals: 322
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3714
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503668952243474e-5
allele num: 66504
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.6e1

DP
type: SiteQuality
SIO_000300: 2.811647e6

GenotypeQuality
all individuals: 3786
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
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GenotypeQuality
all individuals: 22
bin: 7.5e0
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GenotypeQuality
all individuals: 3570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1901
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9365
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29246
bin: 9.75e1
variant carriers: 1

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66472
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.903e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

QD
type: SiteQuality
SIO_000300: 1.111e1

VQSLOD
type: SiteQuality
SIO_000300: -8.179e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.425e0

DP
type: SiteQuality
SIO_000300: 2.804407e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66390
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.213495712687958e-5
allele num: 16094
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

FS
type: SiteQuality
SIO_000300: 6.146e0

QD
type: SiteQuality
SIO_000300: 1.343e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.25e-2

DP
type: SiteQuality
SIO_000300: 2.779269e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16016
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507386192342478e-5
allele num: 66340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 5.83e-1

QD
type: SiteQuality
SIO_000300: 1.214e1

FS
type: SiteQuality
SIO_000300: 3.468e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 2.777744e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQRankSum
type: SiteQuality
SIO_000300: -4.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.092e0

GenotypeQuality
all individuals: 3774
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3665
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.5e0
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GenotypeQuality
all individuals: 1867
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3446
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3049
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15760
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.706853038245001e-5
allele num: 10302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66208
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.495e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.4e-2

DP
type: SiteQuality
SIO_000300: 2.765171e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.44e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.322e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.075782786265316e-5
allele num: 66110
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.984e1

DP
type: SiteQuality
SIO_000300: 1.826093e6

VQSLOD
type: SiteQuality
SIO_000300: 5.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.57e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.52e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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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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variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51290508033526e-5
allele num: 66098
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.837552e6

MQRankSum
type: SiteQuality
SIO_000300: 8.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.987e0

VQSLOD
type: SiteQuality
SIO_000300: 3.75e-1

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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: 6.122199093914534e-5
allele num: 16334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.851049e6

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.445e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66174
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.178967224711153e-4
allele num: 8482
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Other
type: Population
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.46e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 1.858878e6

FS
type: SiteQuality
SIO_000300: 7.308e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.52e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.110975311659741e-5
allele num: 16364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.438e1

MQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 9.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.58e-1

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.864293e6

FS
type: SiteQuality
SIO_000300: 2.978e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008514094888535e-5
allele num: 66478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.0960741282614e-5
allele num: 16404
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.5e-1

FS
type: SiteQuality
SIO_000300: 5.814e0

DP
type: SiteQuality
SIO_000300: 1.884812e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 5.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

QD
type: SiteQuality
SIO_000300: 1.187e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503895088278642e-5
allele num: 66494
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16408
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.886218e6

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.46e-1

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.254e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e-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: 0

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.892066e6

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.075e0

FS
type: SiteQuality
SIO_000300: 2.699e0

QD
type: SiteQuality
SIO_000300: 1.332e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.631e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.35e0

VQSLOD
type: SiteQuality
SIO_000300: 4.18e-1

MQ
type: SiteQuality
SIO_000300: 5.91e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.099e0

MQRankSum
type: SiteQuality
SIO_000300: -2.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.892804e6

QD
type: SiteQuality
SIO_000300: 1.446e1

FS
type: SiteQuality
SIO_000300: 2.22e0

GenotypeQuality
all individuals: 3131
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 21
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002371873780286e-5
allele num: 66614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.46e0

QD
type: SiteQuality
SIO_000300: 1.18e1

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

FS
type: SiteQuality
SIO_000300: 7.02e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.893516e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.22e-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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GenotypeQuality
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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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.893676e6

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.539e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.501530520376928e-5
allele num: 66644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.574e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.499e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.896635e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

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

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

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

South Asian
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allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.272e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.205e0

MQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.17e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.331e1

MQ
type: SiteQuality
SIO_000300: 5.888e1

DP
type: SiteQuality
SIO_000300: 1.89641e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.002400960384154e-5
allele num: 66640
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

DP
type: SiteQuality
SIO_000300: 1.896661e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.683e0

FS
type: SiteQuality
SIO_000300: 1.746e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 19
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variant carriers: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.424536307431204e-4
allele num: 16498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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Other
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African
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European (Finnish)
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European (Non-Finnish)
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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FS
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QD
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DP
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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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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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allele num: 66640
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African
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South Asian
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European (Finnish)
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Other
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FS
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QD
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MQRankSum
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BaseQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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African
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Latino
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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DP
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QD
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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African
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Latino
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ReadPosRankSum
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DP
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele num: 66632
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South Asian
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allele num: 16498
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African
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East Asian
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allele frequency: 0.0e0
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Latino
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Other
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European (Finnish)
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allele frequency: 0.0e0
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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QD
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ClippingRankSum
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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Other
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Latino
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South Asian
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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Other
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South Asian
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African
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European (Finnish)
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ReadPosRankSum
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BaseQRankSum
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DP
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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MQRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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MQ
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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East Asian
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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East Asian
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African
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FS
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.892645e6

VQSLOD
type: SiteQuality
SIO_000300: -7.692e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.283e0

QD
type: SiteQuality
SIO_000300: 9.18e0

GenotypeQuality
all individuals: 3125
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1357
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2224
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503940323647958e-5
allele num: 66492
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.07e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e0

FS
type: SiteQuality
SIO_000300: 6.65e-1

DP
type: SiteQuality
SIO_000300: 1.892272e6

QD
type: SiteQuality
SIO_000300: 1.216e1

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

GenotypeQuality
all individuals: 7857
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.016666165277819e-5
allele num: 66482
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.853e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.67e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.95e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 9.26e0

DP
type: SiteQuality
SIO_000300: 1.89225e6

GenotypeQuality
all individuals: 560
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1357
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.198e0

VQSLOD
type: SiteQuality
SIO_000300: 8.120000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.63e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.181e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 1.368e1

DP
type: SiteQuality
SIO_000300: 1.888419e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
all individuals: 7753
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 5
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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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variant carriers: 0

GenotypeQuality
all individuals: 29511
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variant carriers: 0

GenotypeQuality
all individuals: 8408
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.778994719342852e-5
allele num: 10226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.28e-1

QD
type: SiteQuality
SIO_000300: 7.72e0

FS
type: SiteQuality
SIO_000300: 9.763e0

MQRankSum
type: SiteQuality
SIO_000300: 7.94e-1

DP
type: SiteQuality
SIO_000300: 1.880958e6

VQSLOD
type: SiteQuality
SIO_000300: -7.361e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

MQ
type: SiteQuality
SIO_000300: 5.641e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 29149
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 211
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GenotypeQuality
all individuals: 2762
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 3111
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.512058066026691e-4
allele num: 8542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

FS
type: SiteQuality
SIO_000300: 1.036e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

QD
type: SiteQuality
SIO_000300: 1.333e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.02e-1

DP
type: SiteQuality
SIO_000300: 1.877229e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28103
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variant carriers: 0

GenotypeQuality
all individuals: 2218
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variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 8406
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variant carriers: 2

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 137
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variant carriers: 0

GenotypeQuality
all individuals: 1357
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3106
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66124
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.218620521569583e-4
allele num: 16412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.57e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.403e1

FS
type: SiteQuality
SIO_000300: 2.158e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

DP
type: SiteQuality
SIO_000300: 1.866983e6

GenotypeQuality
all individuals: 856
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2692
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variant carriers: 0

GenotypeQuality
all individuals: 344
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8405
bin: 9.75e1
variant carriers: 9

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.491153142159853e-4
allele num: 16390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.836132e6

QD
type: SiteQuality
SIO_000300: 1.307e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.068e0

MQRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.529e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.62e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
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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: 8400
bin: 9.75e1
variant carriers: 8

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

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

East Asian
type: Population
allele count: 8
allele frequency: 9.46969696969697e-4
allele num: 8448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65842
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.219e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.88e-1

DP
type: SiteQuality
SIO_000300: 1.804318e6

QD
type: SiteQuality
SIO_000300: 1.689e1

FS
type: SiteQuality
SIO_000300: 1.599e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.49e-1

GenotypeQuality
all individuals: 2325
bin: 2.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3892
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521699433927811e-5
allele num: 65716
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10030
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.195e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.33e0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.788731e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.921e-1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 293
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variant carriers: 0

GenotypeQuality
all individuals: 458
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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: 17
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.874e0

DP
type: SiteQuality
SIO_000300: 5.490959e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 1.393e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.272e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

FS
type: SiteQuality
SIO_000300: 1.294e0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e-1

GenotypeQuality
all individuals: 351
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 297
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57962
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.452e1

DP
type: SiteQuality
SIO_000300: 5.491187e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 6.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

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

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

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

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

GenotypeQuality
all individuals: 395
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 621
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.724e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.109e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.883e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.922e0

DP
type: SiteQuality
SIO_000300: 5.49174e6

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

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57967
bin: 9.75e1
variant carriers: 62

GenotypeQuality
all individuals: 395
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 60
allele frequency: 5.765904285988853e-3
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.281e0

MQRankSum
type: SiteQuality
SIO_000300: 1.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.31e-1

DP
type: SiteQuality
SIO_000300: 5.495257e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.35e1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

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

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 304
bin: 6.75e1
variant carriers: 0

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