6-102069779-GTTTA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069779
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069775
    reference: chr 6
allele count: 6
allele frequency: 6.967346370012541e-5
allele num: 86116
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-42_116-39delTATT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-42_116-39delTATT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-42_116-39delTATT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-42_116-39delTATT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-42_116-39delTATT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-42_-32-39delTATT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-42_116-39delTATT
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13996
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17452
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8671
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2671
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3782
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2274
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: GTTTA
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-102069784-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069784
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069784
    reference: chr 6
allele count: 1
allele frequency: 1.149372442646315e-5
allele num: 87004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-40T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-40T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-40T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-40T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-40T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-40T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-40T>C
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5936
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4491
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2247
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7466
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

6-102069785-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069785
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069785
    reference: chr 6
allele count: 1
allele frequency: 1.145790366194601e-5
allele num: 87276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-39T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-39T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-39T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-39T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-39T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-39T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-39T>A
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16612
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12728
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5762
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4476
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 893
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 907
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP

6-102069788-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069788
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069788
    reference: chr 6
allele count: 1
allele frequency: 1.139263580021874e-5
allele num: 87776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-36T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-36T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-36T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-36T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-36T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-36T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-36T>G
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14130
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5770
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4305
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2657
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4930
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13367
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2278
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16123
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS

http://identifiers.org/exac.variant/6-102069792-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069792
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069792
    reference: chr 6
allele count: 74
allele frequency: 8.285746277012652e-4
allele num: 89310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-32A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-32A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-32A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-32A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-32A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-32A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-32A>C
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12476
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 14271
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18392
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6144
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3922
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20235
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3047
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3551
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/6-102069794-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069794
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069794
    reference: chr 6
allele count: 1
allele frequency: 1.104508604122026e-5
allele num: 90538
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-30A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-30A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-30A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-30A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-30A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-30A>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-30A>C
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20932
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14001
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3260
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13393
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2871
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2299
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

6-102069795-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069795
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069795
    reference: chr 6
allele count: 423
allele frequency: 4.641720618896082e-3
allele num: 91130
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-29T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-29T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-29T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-29T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-29T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-29T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-29T>G
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 2.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13762
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 10181
  bin: 1.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 3.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21791
  bin: 2.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 1.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4821
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22957
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2616
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13172
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 1.75e1
  variant carriers: 1
num of homozygotes: 3
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

6-102069800-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069800
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069800
    reference: chr 6
allele count: 1
allele frequency: 1.04760308414348e-5
allele num: 95456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-24G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-24G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-24G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-24G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-24G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-24G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-24G>T
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 27600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11863
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2349
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3724
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11723
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

6-102069804-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069804
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069804
    reference: chr 6
allele count: 1
allele frequency: 1.005227181342983e-5
allele num: 99480
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-20T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-20T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-20T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-20T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-20T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-20T>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-20T>A
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30883
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10147
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4112
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

6-102069805-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069805
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069803
    reference: chr 6
allele count: 1
allele frequency: 9.929894941711517e-6
allele num: 100706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-15_-32-14delCT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-15_116-14delCT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-15_116-14delCT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-15_116-14delCT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-15_116-14delCT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-15_116-14delCT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-15_116-14delCT
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9727
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2366
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4249
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: TTC
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

6-102069807-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069807
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069807
    reference: chr 6
allele count: 1
allele frequency: 9.718172983479106e-6
allele num: 102900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-17C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-17C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-17C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-17C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-17C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-17C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-17C>T
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8624
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1552
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

6-102069807-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069807
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069807
    reference: chr 6
allele count: 1
allele frequency: 9.718172983479106e-6
allele num: 102900
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-17C>G
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1398
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-102069809-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069809
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069809
    reference: chr 6
allele count: 2
allele frequency: 1.898037429298106e-5
allele num: 105372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-15C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-15C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-15C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-15C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-15C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-15C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-15C>T
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7578
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2377
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

6-102069818-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069818
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069817
    reference: chr 6
allele count: 1
allele frequency: 8.793682618406936e-6
allele num: 113718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-5delG
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-5delG
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-5delG
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-5delG
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-5delG
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-5delG
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-5delG
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9153
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3701
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 9.25e1
  variant carriers: 0
hgvs: c.116-5delG
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: TG
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/6-102069820-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069820
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069820
    reference: chr 6
allele count: 1
allele frequency: 8.699888641425389e-6
allele num: 114944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-4C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-4C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-4C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-4C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-4C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-4C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-4C>A
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3089
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42752
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
hgvs: c.116-4C>A
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

6-102069820-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069820
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069820
    reference: chr 6
allele count: 1
allele frequency: 8.699888641425389e-6
allele num: 114944
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.116-4C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.116-4C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.116-4C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.116-4C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.116-4C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-32-4C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.116-4C>T
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9451
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42752
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1013
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3089
  bin: 2.25e1
  variant carriers: 0
hgvs: c.116-4C>T
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

6-102069826-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069826
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069826
    reference: chr 6
allele count: 2
allele frequency: 1.700217627856366e-5
allele num: 117632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.118G>A
  hgvsp: ENSP00000405596.1:p.Gly40Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.118G>A
  hgvsp: ENSP00000313276.6:p.Gly40Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.118G>A
  hgvsp: ENSP00000397026.1:p.Gly40Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-30G>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.118G>A
  hgvsp: ENSP00000358134.1:p.Gly40Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.118G>A
  hgvsp: ENSP00000351128.3:p.Gly40Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.118G>A
  hgvsp: ENSP00000358133.3:p.Gly40Ser
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1811
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly40Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

6-102069827-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069827
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069827
    reference: chr 6
allele count: 1
allele frequency: 8.482051978014521e-6
allele num: 117896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.119G>T
  hgvsp: ENSP00000405596.1:p.Gly40Val
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.119G>T
  hgvsp: ENSP00000397026.1:p.Gly40Val
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.119G>T
  hgvsp: ENSP00000313276.6:p.Gly40Val
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.119G>T
  hgvsp: ENSP00000358133.3:p.Gly40Val
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.119G>T
  hgvsp: ENSP00000351128.3:p.Gly40Val
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-29G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.119G>T
  hgvsp: ENSP00000358134.1:p.Gly40Val
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44317
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly40Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-102069847-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069847
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069847
    reference: chr 6
allele count: 1
allele frequency: 8.326671995736744e-6
allele num: 120096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.139T>A
  hgvsp: ENSP00000405596.1:p.Ser47Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.139T>A
  hgvsp: ENSP00000358133.3:p.Ser47Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.139T>A
  hgvsp: ENSP00000358134.1:p.Ser47Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.139T>A
  hgvsp: ENSP00000351128.3:p.Ser47Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.139T>A
  hgvsp: ENSP00000397026.1:p.Ser47Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.139T>A
  hgvsp: ENSP00000313276.6:p.Ser47Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.-9T>A
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1590
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser47Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

6-102069858-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069858
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069858
    reference: chr 6
allele count: 1
allele frequency: 8.302475798283047e-6
allele num: 120446
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.3G>A
  hgvsp: ENSP00000358130.4:p.Met1?
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.150G>A
  hgvsp: ENSP00000313276.6:p.Met50Ile
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.150G>A
  hgvsp: ENSP00000351128.3:p.Met50Ile
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.150G>A
  hgvsp: ENSP00000405596.1:p.Met50Ile
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.150G>A
  hgvsp: ENSP00000397026.1:p.Met50Ile
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.150G>A
  hgvsp: ENSP00000358134.1:p.Met50Ile
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.150G>A
  hgvsp: ENSP00000358133.3:p.Met50Ile
  variant of: http://identifiers.org/hgnc/4580
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD

6-102069860-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069860
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069860
    reference: chr 6
allele count: 1
allele frequency: 8.300683976359652e-6
allele num: 120472
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.152G>A
  hgvsp: ENSP00000405596.1:p.Gly51Glu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.152G>A
  hgvsp: ENSP00000397026.1:p.Gly51Glu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.152G>A
  hgvsp: ENSP00000313276.6:p.Gly51Glu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.152G>A
  hgvsp: ENSP00000351128.3:p.Gly51Glu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.152G>A
  hgvsp: ENSP00000358134.1:p.Gly51Glu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.5G>A
  hgvsp: ENSP00000358130.4:p.Gly2Glu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.152G>A
  hgvsp: ENSP00000358133.3:p.Gly51Glu
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45788
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly51Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/6-102069870-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069870
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069870
    reference: chr 6
allele count: 1
allele frequency: 8.290636555074699e-6
allele num: 120618
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.162A>C
  hgvsp: ENSP00000397026.1:p.Glu54Asp
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.162A>C
  hgvsp: ENSP00000358134.1:p.Glu54Asp
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.162A>C
  hgvsp: ENSP00000313276.6:p.Glu54Asp
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.162A>C
  hgvsp: ENSP00000358133.3:p.Glu54Asp
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.162A>C
  hgvsp: ENSP00000351128.3:p.Glu54Asp
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.15A>C
  hgvsp: ENSP00000358130.4:p.Glu5Asp
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.162A>C
  hgvsp: ENSP00000405596.1:p.Glu54Asp
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu54Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-102069913-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069913
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069913
    reference: chr 6
allele count: 1
allele frequency: 8.269656974628692e-6
allele num: 120924
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.205A>G
  hgvsp: ENSP00000358134.1:p.Thr69Ala
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.205A>G
  hgvsp: ENSP00000358133.3:p.Thr69Ala
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.205A>G
  hgvsp: ENSP00000397026.1:p.Thr69Ala
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.205A>G
  hgvsp: ENSP00000351128.3:p.Thr69Ala
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.205A>G
  hgvsp: ENSP00000405596.1:p.Thr69Ala
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.58A>G
  hgvsp: ENSP00000358130.4:p.Thr20Ala
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.205A>G
  hgvsp: ENSP00000313276.6:p.Thr69Ala
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46140
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr69Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

6-102069916-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069916
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069916
    reference: chr 6
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.208T>C
  hgvsp: ENST00000369137.3:c.208T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.208T>C
  hgvsp: ENST00000369138.1:c.208T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.208T>C
  hgvsp: ENST00000421544.1:c.208T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.208T>C
  hgvsp: ENST00000413795.1:c.208T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.61T>C
  hgvsp: ENST00000369134.4:c.61T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.208T>C
  hgvsp: ENST00000318991.6:c.208T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.208T>C
  hgvsp: ENST00000358361.3:c.208T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46169
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu70Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

6-102069919-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069919
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069919
    reference: chr 6
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.211C>T
  hgvsp: ENST00000421544.1:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.211C>T
  hgvsp: ENST00000318991.6:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.211C>T
  hgvsp: ENST00000369138.1:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.211C>T
  hgvsp: ENST00000369137.3:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.64C>T
  hgvsp: ENST00000369134.4:c.64C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.211C>T
  hgvsp: ENST00000413795.1:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.211C>T
  hgvsp: ENST00000358361.3:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu71Leu
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

6-102069923-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069923
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069923
    reference: chr 6
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.215C>G
  hgvsp: ENSP00000313276.6:p.Pro72Arg
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.215C>G
  hgvsp: ENSP00000397026.1:p.Pro72Arg
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.215C>G
  hgvsp: ENSP00000358133.3:p.Pro72Arg
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.215C>G
  hgvsp: ENSP00000351128.3:p.Pro72Arg
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.215C>G
  hgvsp: ENSP00000405596.1:p.Pro72Arg
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.215C>G
  hgvsp: ENSP00000358134.1:p.Pro72Arg
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.68C>G
  hgvsp: ENSP00000358130.4:p.Pro23Arg
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro72Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

6-102069939-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069939
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069939
    reference: chr 6
allele count: 2
allele frequency: 1.653111155194075e-5
allele num: 120984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.231C>T
  hgvsp: ENST00000358361.3:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.231C>T
  hgvsp: ENST00000413795.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.231C>T
  hgvsp: ENST00000318991.6:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.231C>T
  hgvsp: ENST00000421544.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.231C>T
  hgvsp: ENST00000369138.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.84C>T
  hgvsp: ENST00000369134.4:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.231C>T
  hgvsp: ENST00000369137.3:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr77Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

6-102069942-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069942
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069942
    reference: chr 6
allele count: 15
allele frequency: 1.239874359398248e-4
allele num: 120980
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.234T>C
  hgvsp: ENST00000421544.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.234T>C
  hgvsp: ENST00000369138.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.234T>C
  hgvsp: ENST00000413795.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.234T>C
  hgvsp: ENST00000358361.3:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.234T>C
  hgvsp: ENST00000369137.3:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.87T>C
  hgvsp: ENST00000369134.4:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.234T>C
  hgvsp: ENST00000318991.6:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11303
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1768
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr78Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-102069958-AACC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069958
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069955
    reference: chr 6
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.251_253delACC
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.251_253delACC
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.251_253delACC
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.251_253delACC
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.251_253delACC
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.104_106delACC
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.251_253delACC
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn84_Leu85delinsIle
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: AACC
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-102069960-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069960
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069960
    reference: chr 6
allele count: 1
allele frequency: 8.269109913008963e-6
allele num: 120932
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.252C>A
  hgvsp: ENSP00000351128.3:p.Asn84Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.105C>A
  hgvsp: ENSP00000358130.4:p.Asn35Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.252C>A
  hgvsp: ENSP00000358134.1:p.Asn84Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.252C>A
  hgvsp: ENSP00000405596.1:p.Asn84Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.252C>A
  hgvsp: ENSP00000313276.6:p.Asn84Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.252C>A
  hgvsp: ENSP00000397026.1:p.Asn84Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.252C>A
  hgvsp: ENSP00000358133.3:p.Asn84Lys
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46290
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn84Lys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-102069961-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069961
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069961
    reference: chr 6
allele count: 1
allele frequency: 8.270067318347971e-6
allele num: 120918
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.253C>A
  hgvsp: ENSP00000397026.1:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.253C>A
  hgvsp: ENSP00000358134.1:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.253C>A
  hgvsp: ENSP00000351128.3:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.253C>A
  hgvsp: ENSP00000358133.3:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.253C>A
  hgvsp: ENSP00000405596.1:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.253C>A
  hgvsp: ENSP00000313276.6:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.106C>A
  hgvsp: ENSP00000358130.4:p.Leu36Ile
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2412
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1582
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu85Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

6-102069969-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069969
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069969
    reference: chr 6
allele count: 2
allele frequency: 1.654697686732634e-5
allele num: 120868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.261T>C
  hgvsp: ENST00000318991.6:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.261T>C
  hgvsp: ENST00000358361.3:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.261T>C
  hgvsp: ENST00000413795.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.261T>C
  hgvsp: ENST00000421544.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.261T>C
  hgvsp: ENST00000369137.3:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.114T>C
  hgvsp: ENST00000369134.4:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.261T>C
  hgvsp: ENST00000369138.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1761
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5964
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp87Asp
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-102069975-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069975
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069975
    reference: chr 6
allele count: 2
allele frequency: 1.655382476121108e-5
allele num: 120818
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.267T>C
  hgvsp: ENST00000358361.3:c.267T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.267T>C
  hgvsp: ENST00000318991.6:c.267T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.120T>C
  hgvsp: ENST00000369134.4:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.267T>C
  hgvsp: ENST00000421544.1:c.267T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.267T>C
  hgvsp: ENST00000369138.1:c.267T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.267T>C
  hgvsp: ENST00000369137.3:c.267T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.267T>C
  hgvsp: ENST00000413795.1:c.267T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46159
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe89Phe
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-102069981-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069981
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069981
    reference: chr 6
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.273A>G
  hgvsp: ENST00000369137.3:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.273A>G
  hgvsp: ENST00000421544.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.273A>G
  hgvsp: ENST00000413795.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.273A>G
  hgvsp: ENST00000318991.6:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.126A>G
  hgvsp: ENST00000369134.4:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.273A>G
  hgvsp: ENST00000358361.3:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.273A>G
  hgvsp: ENST00000369138.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1756
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5958
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala91Ala
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

6-102069984-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069984
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069984
    reference: chr 6
allele count: 1
allele frequency: 8.288300235387727e-6
allele num: 120652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.276C>T
  hgvsp: ENST00000369138.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.276C>T
  hgvsp: ENST00000318991.6:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.276C>T
  hgvsp: ENST00000358361.3:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.129C>T
  hgvsp: ENST00000369134.4:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.276C>T
  hgvsp: ENST00000369137.3:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.276C>T
  hgvsp: ENST00000421544.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.276C>T
  hgvsp: ENST00000413795.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1581
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45939
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1093
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser92Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

6-102069996-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102069996
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102069996
    reference: chr 6
allele count: 1
allele frequency: 8.314901967305805e-6
allele num: 120266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.283+5T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.283+5T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.283+5T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.283+5T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.283+5T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.283+5T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.136+5T>C
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 40335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11084
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.25e1
  variant carriers: 0
hgvs: c.283+5T>C
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

6-102070003-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102070003
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102070004
    reference: chr 6
allele count: 1
allele frequency: 8.325008325008325e-6
allele num: 120120
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.136+17dupT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.283+17dupT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.283+17dupT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.283+17dupT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.283+17dupT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.283+17dupT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.283+17dupT
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44854
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

6-102070004-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102070004
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102070004
    reference: chr 6
allele count: 1
allele frequency: 8.325701440346349e-6
allele num: 120110
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.283+13T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.283+13T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.136+13T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.283+13T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.283+13T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.283+13T>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.283+13T>G
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5856
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

6-102070012-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102070012
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102070011
    reference: chr 6
allele count: 1
allele frequency: 8.347942232239753e-6
allele num: 119790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.283+22delT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.283+22delT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.283+22delT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.283+22delT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.283+22delT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.136+22delT
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.283+22delT
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1523
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5653
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: AT
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

6-102070018-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102070018
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102070018
    reference: chr 6
allele count: 1
allele frequency: 8.372965369415233e-6
allele num: 119432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.136+27G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.283+27G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.283+27G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.283+27G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.283+27G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.283+27G>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.283+27G>T
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

6-102070023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102070023
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102070023
    reference: chr 6
allele count: 2
allele frequency: 1.678021277309796e-5
allele num: 119188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.283+32C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.136+32C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.283+32C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.283+32C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.283+32C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.283+32C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.283+32C>T
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2485
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5384
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

6-102070039-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102070039
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102070039
    reference: chr 6
allele count: 9
allele frequency: 7.67067246228586e-5
allele num: 117330
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.283+48T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.136+48T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.283+48T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.283+48T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.283+48T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.283+48T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.283+48T>C
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9660
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3011
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1619
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2492
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3762
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

6-102074205-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074205
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074205
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 115704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.284-50A>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.284-50A>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.284-50A>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.284-50A>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.284-50A>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.137-50A>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.284-50A>T
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1679
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2526
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29178
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

6-102074223-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074223
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074223
    reference: chr 6
allele count: 1
allele frequency: 8.608222574202878e-6
allele num: 116168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.137-32T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.284-32T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.284-32T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.284-32T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.284-32T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.284-32T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.284-32T>C
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7200
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29903
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3284
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2537
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2227
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

6-102074226-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074226
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074226
    reference: chr 6
allele count: 1
allele frequency: 8.598452278589854e-6
allele num: 116300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.284-29T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.284-29T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.284-29T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.284-29T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.284-29T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.284-29T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.137-29T>C
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2226
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30072
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7202
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

6-102074230-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074230
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074230
    reference: chr 6
allele count: 1
allele frequency: 8.590327291469806e-6
allele num: 116410
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.284-25T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.284-25T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.284-25T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.284-25T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.284-25T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.137-25T>C
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.284-25T>C
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30328
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7201
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2319
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/6-102074237-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074237
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074237
    reference: chr 6
allele count: 2
allele frequency: 1.710629853912211e-5
allele num: 116916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.284-18C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.137-18C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.284-18C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.284-18C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.284-18C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.284-18C>A
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.284-18C>A
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30817
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP

6-102074237-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074237
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074237
    reference: chr 6
allele count: 2
allele frequency: 1.710629853912211e-5
allele num: 116916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.137-18C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.284-18C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.284-18C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.284-18C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.284-18C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.284-18C>T
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.284-18C>T
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2153
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3292
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8067
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

6-102074238-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074238
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074238
    reference: chr 6
allele count: 31
allele frequency: 2.648757647219659e-4
allele num: 117036
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.284-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.284-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.284-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.284-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.284-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.284-17C>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.137-17C>G
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14986
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8076
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3289
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7203
  bin: 9.75e1
  variant carriers: 31
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

6-102074242-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074242
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074242
    reference: chr 6
allele count: 2057
allele frequency: 1.749090167001122e-2
allele num: 117604
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.284-13A>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.284-13A>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.284-13A>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.284-13A>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.284-13A>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.137-13A>G
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.284-13A>G
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 2.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 22848
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 9.75e1
  variant carriers: 1768
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 14993
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31401
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8088
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2230
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1910
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 28
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

6-102074266-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074266
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074266
    reference: chr 6
allele count: 1
allele frequency: 8.307993951780402e-6
allele num: 120366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.295C>T
  hgvsp: ENST00000318991.6:c.295C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.295C>T
  hgvsp: ENST00000358361.3:c.295C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.295C>T
  hgvsp: ENST00000369138.1:c.295C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.295C>T
  hgvsp: ENST00000413795.1:c.295C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.295C>T
  hgvsp: ENST00000421544.1:c.295C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.295C>T
  hgvsp: ENST00000369137.3:c.295C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.148C>T
  hgvsp: ENST00000369134.4:c.148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3428
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2646
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu99Leu
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-102074276-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074276
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074276
    reference: chr 6
allele count: 1
allele frequency: 8.277049397430804e-6
allele num: 120816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.305G>T
  hgvsp: ENSP00000351128.3:p.Gly102Val
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.305G>T
  hgvsp: ENSP00000313276.6:p.Gly102Val
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.305G>T
  hgvsp: ENSP00000397026.1:p.Gly102Val
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.305G>T
  hgvsp: ENSP00000405596.1:p.Gly102Val
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.305G>T
  hgvsp: ENSP00000358134.1:p.Gly102Val
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.158G>T
  hgvsp: ENSP00000358130.4:p.Gly53Val
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.305G>T
  hgvsp: ENSP00000358133.3:p.Gly102Val
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2656
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5556
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly102Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

6-102074280-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074280
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074280
    reference: chr 6
allele count: 3
allele frequency: 2.480568877129155e-5
allele num: 120940
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.162G>T
  hgvsp: ENST00000369134.4:c.162G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.309G>T
  hgvsp: ENST00000369138.1:c.309G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.309G>T
  hgvsp: ENST00000318991.6:c.309G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.309G>T
  hgvsp: ENST00000413795.1:c.309G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.309G>T
  hgvsp: ENST00000421544.1:c.309G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.309G>T
  hgvsp: ENST00000358361.3:c.309G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.309G>T
  hgvsp: ENST00000369137.3:c.309G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2663
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val103Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-102074286-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074286
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074286
    reference: chr 6
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.315C>A
  hgvsp: ENST00000358361.3:c.315C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.315C>A
  hgvsp: ENST00000369138.1:c.315C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.315C>A
  hgvsp: ENST00000421544.1:c.315C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.168C>A
  hgvsp: ENST00000369134.4:c.168C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.315C>A
  hgvsp: ENST00000318991.6:c.315C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.315C>A
  hgvsp: ENST00000369137.3:c.315C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.315C>A
  hgvsp: ENST00000413795.1:c.315C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5553
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35570
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala105Ala
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

6-102074292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074292
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074292
    reference: chr 6
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.321C>T
  hgvsp: ENST00000421544.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.174C>T
  hgvsp: ENST00000369134.4:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.321C>T
  hgvsp: ENST00000358361.3:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.321C>T
  hgvsp: ENST00000369138.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.321C>T
  hgvsp: ENST00000318991.6:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.321C>T
  hgvsp: ENST00000413795.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.321C>T
  hgvsp: ENST00000369137.3:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe107Phe
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

6-102074304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074304
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074304
    reference: chr 6
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.333C>T
  hgvsp: ENST00000421544.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.333C>T
  hgvsp: ENST00000318991.6:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.333C>T
  hgvsp: ENST00000369137.3:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.333C>T
  hgvsp: ENST00000358361.3:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.333C>T
  hgvsp: ENST00000369138.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.333C>T
  hgvsp: ENST00000413795.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.186C>T
  hgvsp: ENST00000369134.4:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5551
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35797
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8558
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His111His
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: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

6-102074309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074309
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074309
    reference: chr 6
allele count: 2
allele frequency: 1.64866870002473e-5
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.338C>T
  hgvsp: ENSP00000358134.1:p.Ser113Leu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.338C>T
  hgvsp: ENSP00000397026.1:p.Ser113Leu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.338C>T
  hgvsp: ENSP00000313276.6:p.Ser113Leu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.338C>T
  hgvsp: ENSP00000405596.1:p.Ser113Leu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.338C>T
  hgvsp: ENSP00000351128.3:p.Ser113Leu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.191C>T
  hgvsp: ENSP00000358130.4:p.Ser64Leu
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.338C>T
  hgvsp: ENSP00000358133.3:p.Ser113Leu
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5548
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2314
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser113Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/6-102074313-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074313
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074313
    reference: chr 6
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.342A>C
  hgvsp: ENST00000369137.3:c.342A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.342A>C
  hgvsp: ENST00000413795.1:c.342A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.342A>C
  hgvsp: ENST00000421544.1:c.342A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.342A>C
  hgvsp: ENST00000358361.3:c.342A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.342A>C
  hgvsp: ENST00000369138.1:c.342A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.195A>C
  hgvsp: ENST00000369134.4:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.342A>C
  hgvsp: ENST00000318991.6:c.342A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8562
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3419
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser114Ser
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

6-102074313-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074313
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074313
    reference: chr 6
allele count: 2
allele frequency: 1.64883180266781e-5
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.342A>T
  hgvsp: ENST00000421544.1:c.342A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.342A>T
  hgvsp: ENST00000369138.1:c.342A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.342A>T
  hgvsp: ENST00000318991.6:c.342A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.195A>T
  hgvsp: ENST00000369134.4:c.195A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.342A>T
  hgvsp: ENST00000369137.3:c.342A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.342A>T
  hgvsp: ENST00000358361.3:c.342A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.342A>T
  hgvsp: ENST00000413795.1:c.342A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35838
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser114Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

6-102074318-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074318
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074318
    reference: chr 6
allele count: 8
allele frequency: 6.594022518586901e-5
allele num: 121322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.347A>G
  hgvsp: ENSP00000358134.1:p.Asn116Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.347A>G
  hgvsp: ENSP00000397026.1:p.Asn116Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.347A>G
  hgvsp: ENSP00000351128.3:p.Asn116Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.347A>G
  hgvsp: ENSP00000405596.1:p.Asn116Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.200A>G
  hgvsp: ENSP00000358130.4:p.Asn67Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.347A>G
  hgvsp: ENSP00000313276.6:p.Asn116Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.347A>G
  hgvsp: ENSP00000358133.3:p.Asn116Ser
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3424
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8557
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn116Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

6-102074319-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074319
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074319
    reference: chr 6
allele count: 4
allele frequency: 3.297065611605671e-5
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.348C>T
  hgvsp: ENST00000369138.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.348C>T
  hgvsp: ENST00000358361.3:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.201C>T
  hgvsp: ENST00000369134.4:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.348C>T
  hgvsp: ENST00000413795.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.348C>T
  hgvsp: ENST00000318991.6:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.348C>T
  hgvsp: ENST00000369137.3:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.348C>T
  hgvsp: ENST00000421544.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn116Asn
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-102074319-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074319
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074319
    reference: chr 6
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.348C>A
  hgvsp: ENSP00000358134.1:p.Asn116Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.348C>A
  hgvsp: ENSP00000313276.6:p.Asn116Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.348C>A
  hgvsp: ENSP00000351128.3:p.Asn116Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.201C>A
  hgvsp: ENSP00000358130.4:p.Asn67Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.348C>A
  hgvsp: ENSP00000405596.1:p.Asn116Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.348C>A
  hgvsp: ENSP00000397026.1:p.Asn116Lys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.348C>A
  hgvsp: ENSP00000358133.3:p.Asn116Lys
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8557
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5536
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn116Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

6-102074320-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074320
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074320
    reference: chr 6
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.349G>A
  hgvsp: ENSP00000397026.1:p.Ala117Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.349G>A
  hgvsp: ENSP00000313276.6:p.Ala117Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.349G>A
  hgvsp: ENSP00000405596.1:p.Ala117Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.349G>A
  hgvsp: ENSP00000358133.3:p.Ala117Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.202G>A
  hgvsp: ENSP00000358130.4:p.Ala68Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.349G>A
  hgvsp: ENSP00000351128.3:p.Ala117Thr
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.349G>A
  hgvsp: ENSP00000358134.1:p.Ala117Thr
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3427
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala117Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

6-102074339-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074339
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074339
    reference: chr 6
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.368A>G
  hgvsp: ENSP00000397026.1:p.Asn123Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.221A>G
  hgvsp: ENSP00000358130.4:p.Asn74Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.368A>G
  hgvsp: ENSP00000405596.1:p.Asn123Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.368A>G
  hgvsp: ENSP00000358134.1:p.Asn123Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.368A>G
  hgvsp: ENSP00000351128.3:p.Asn123Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.368A>G
  hgvsp: ENSP00000313276.6:p.Asn123Ser
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.368A>G
  hgvsp: ENSP00000358133.3:p.Asn123Ser
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35877
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2654
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn123Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

6-102074342-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074342
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074342
    reference: chr 6
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.371C>G
  hgvsp: ENSP00000405596.1:p.Ala124Gly
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.371C>G
  hgvsp: ENSP00000313276.6:p.Ala124Gly
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.371C>G
  hgvsp: ENSP00000397026.1:p.Ala124Gly
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.371C>G
  hgvsp: ENSP00000358133.3:p.Ala124Gly
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.224C>G
  hgvsp: ENSP00000358130.4:p.Ala75Gly
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.371C>G
  hgvsp: ENSP00000351128.3:p.Ala124Gly
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.371C>G
  hgvsp: ENSP00000358134.1:p.Ala124Gly
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5528
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3422
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8554
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35884
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala124Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

6-102074349-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074349
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074349
    reference: chr 6
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.378A>T
  hgvsp: ENST00000413795.1:c.378A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.378A>T
  hgvsp: ENST00000369138.1:c.378A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.378A>T
  hgvsp: ENST00000421544.1:c.378A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.378A>T
  hgvsp: ENST00000318991.6:c.378A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.378A>T
  hgvsp: ENST00000358361.3:c.378A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.231A>T
  hgvsp: ENST00000369134.4:c.231A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.378A>T
  hgvsp: ENST00000369137.3:c.378A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly126Gly
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

6-102074361-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074361
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074361
    reference: chr 6
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.390A>G
  hgvsp: ENSP00000313276.6:p.Ile130Met
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.390A>G
  hgvsp: ENSP00000351128.3:p.Ile130Met
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.390A>G
  hgvsp: ENSP00000397026.1:p.Ile130Met
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.243A>G
  hgvsp: ENSP00000358130.4:p.Ile81Met
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.390A>G
  hgvsp: ENSP00000405596.1:p.Ile130Met
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.390A>G
  hgvsp: ENSP00000358133.3:p.Ile130Met
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.390A>G
  hgvsp: ENSP00000358134.1:p.Ile130Met
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3417
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8560
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile130Met
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

6-102074368-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074368
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074368
    reference: chr 6
allele count: 3
allele frequency: 2.472595400972554e-5
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.397C>T
  hgvsp: ENSP00000405596.1:p.Arg133Cys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.397C>T
  hgvsp: ENSP00000313276.6:p.Arg133Cys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.397C>T
  hgvsp: ENSP00000358134.1:p.Arg133Cys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.397C>T
  hgvsp: ENSP00000397026.1:p.Arg133Cys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.250C>T
  hgvsp: ENSP00000358130.4:p.Arg84Cys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.397C>T
  hgvsp: ENSP00000351128.3:p.Arg133Cys
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.397C>T
  hgvsp: ENSP00000358133.3:p.Arg133Cys
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25043
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5523
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 35881
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8560
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg133Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/6-102074370-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074370
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074370
    reference: chr 6
allele count: 3
allele frequency: 2.472473132458627e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.399C>A
  hgvsp: ENST00000413795.1:c.399C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.399C>A
  hgvsp: ENST00000421544.1:c.399C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.399C>A
  hgvsp: ENST00000318991.6:c.399C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.252C>A
  hgvsp: ENST00000369134.4:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.399C>A
  hgvsp: ENST00000358361.3:c.399C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.399C>A
  hgvsp: ENST00000369137.3:c.399C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.399C>A
  hgvsp: ENST00000369138.1:c.399C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3417
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg133Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

6-102074370-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074370
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074370
    reference: chr 6
allele count: 3
allele frequency: 2.472473132458627e-5
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.399C>T
  hgvsp: ENST00000358361.3:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.399C>T
  hgvsp: ENST00000413795.1:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.399C>T
  hgvsp: ENST00000421544.1:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.399C>T
  hgvsp: ENST00000369137.3:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.399C>T
  hgvsp: ENST00000369138.1:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.399C>T
  hgvsp: ENST00000318991.6:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.252C>T
  hgvsp: ENST00000369134.4:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg133Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS

6-102074376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074376
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074376
    reference: chr 6
allele count: 5
allele frequency: 4.121060266385336e-5
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.405G>A
  hgvsp: ENST00000358361.3:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.258G>A
  hgvsp: ENST00000369134.4:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.405G>A
  hgvsp: ENST00000413795.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.405G>A
  hgvsp: ENST00000421544.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.405G>A
  hgvsp: ENST00000318991.6:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.405G>A
  hgvsp: ENST00000369138.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.405G>A
  hgvsp: ENST00000369137.3:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8544
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys135Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

6-102074382-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102074382
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 102074382
    reference: chr 6
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000313276
  ensembl transcript: ENST00000318991
  gene symbol: GRIK2
  hgvsc: ENST00000318991.6:c.411G>C
  hgvsp: ENSP00000313276.6:p.Gln137His
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000405596
  ensembl transcript: ENST00000413795
  gene symbol: GRIK2
  hgvsc: ENST00000413795.1:c.411G>C
  hgvsp: ENSP00000405596.1:p.Gln137His
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358130
  ensembl transcript: ENST00000369134
  gene symbol: GRIK2
  hgvsc: ENST00000369134.4:c.264G>C
  hgvsp: ENSP00000358130.4:p.Gln88His
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358134
  ensembl transcript: ENST00000369138
  gene symbol: GRIK2
  hgvsc: ENST00000369138.1:c.411G>C
  hgvsp: ENSP00000358134.1:p.Gln137His
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000358133
  ensembl transcript: ENST00000369137
  gene symbol: GRIK2
  hgvsc: ENST00000369137.3:c.411G>C
  hgvsp: ENSP00000358133.3:p.Gln137His
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000351128
  ensembl transcript: ENST00000358361
  gene symbol: GRIK2
  hgvsc: ENST00000358361.3:c.411G>C
  hgvsp: ENSP00000351128.3:p.Gln137His
  variant of: http://identifiers.org/hgnc/4580
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164418
  ensembl protein: ENSP00000397026
  ensembl transcript: ENST00000421544
  gene symbol: GRIK2
  hgvsc: ENST00000421544.1:c.411G>C
  hgvsp: ENSP00000397026.1:p.Gln137His
  variant of: http://identifiers.org/hgnc/4580
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln137His
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 705
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10837
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6349
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4539
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7577
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.206141899046947e-5
allele num: 45328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5088
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 6.973500697350069e-4
allele num: 7170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5660
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13708
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.021e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.82172e5

VQSLOD
type: SiteQuality
SIO_000300: 3.6e0

MQ
type: SiteQuality
SIO_000300: 5.73e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.67e-1

GenotypeQuality
all individuals: 756
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12507
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2397
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12512
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2513
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5716
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.170686022008897e-4
allele num: 8542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13792
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.009312e6

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 772
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13128
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2458
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5724
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.175237100843992e-5
allele num: 45972
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7256
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.76e0

VQSLOD
type: SiteQuality
SIO_000300: -3.883e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.344e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.344e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

DP
type: SiteQuality
SIO_000300: 1.01625e6

GenotypeQuality
all individuals: 402
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1604
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1499
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6985
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5736
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.912777352716144e-4
allele num: 5228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46278
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.957e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 1.045375e6

MQRankSum
type: SiteQuality
SIO_000300: -3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 5849
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 371
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13537
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 645
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2355
bin: 9.75e1
variant carriers: 73

European (Non-Finnish)
type: Population
allele count: 48
allele frequency: 1.017423375302048e-3
allele num: 47178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 20
allele frequency: 3.457814661134163e-3
allele num: 5784
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.302083333333333e-3
allele num: 768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5378
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 5.688282138794084e-4
allele num: 8790
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13982
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

QD
type: SiteQuality
SIO_000300: 1.546e1

DP
type: SiteQuality
SIO_000300: 1.09266e6

VQSLOD
type: SiteQuality
SIO_000300: 4.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 442
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22439
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47848
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14082
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.802451333813987e-4
allele num: 5548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8940
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5832
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

DP
type: SiteQuality
SIO_000300: 1.121366e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.659e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -8.08e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

QD
type: SiteQuality
SIO_000300: 1.208e1

GenotypeQuality
all individuals: 3453
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 166
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 974
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3321
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 647
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 431
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1085
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2685
bin: 9.75e1
variant carriers: 415

European (Non-Finnish)
type: Population
allele count: 241
allele frequency: 4.996475515196749e-3
allele num: 48234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 172
allele frequency: 2.93615568453397e-2
allele num: 5858
num of homozygotes: 3

Other
type: Population
allele count: 3
allele frequency: 3.856041131105398e-3
allele num: 778
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.345227475468332e-4
allele num: 8968
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5596
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 5.282620179609086e-4
allele num: 7572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14124
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

QD
type: SiteQuality
SIO_000300: 1.663e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.136603e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

GenotypeQuality
all individuals: 3083
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2497
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29066
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7938
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.970676336118556e-5
allele num: 50744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6010
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.214938e6

VQSLOD
type: SiteQuality
SIO_000300: -3.437e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.236e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.973e0

GenotypeQuality
all individuals: 611
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2186
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1895
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2365
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 386
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31800
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9820
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53092
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.541782300339192e-4
allele num: 6486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.418e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.813e0

VQSLOD
type: SiteQuality
SIO_000300: -1.228e0

FS
type: SiteQuality
SIO_000300: 4.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e0

DP
type: SiteQuality
SIO_000300: 1.264895e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

QD
type: SiteQuality
SIO_000300: 9.16e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33258
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14970
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.856596487319446e-5
allele num: 53862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.814e1

MQ
type: SiteQuality
SIO_000300: 6.022e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.227e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.74e-1

FS
type: SiteQuality
SIO_000300: 3.559e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.79e-1

DP
type: SiteQuality
SIO_000300: 1.279078e6

GenotypeQuality
all individuals: 426
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 840
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.812382195157315e-5
allele num: 55176
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15152
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.694e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.334e0

DP
type: SiteQuality
SIO_000300: 1.309162e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.32e-1

QD
type: SiteQuality
SIO_000300: 1.175e1

VQSLOD
type: SiteQuality
SIO_000300: 6.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-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
all individuals: 368
bin: 4.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15152
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.812382195157315e-5
allele num: 55176
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6852
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.309162e6

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.32e-1

FS
type: SiteQuality
SIO_000300: 1.694e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.36e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.334e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8792
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6262
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7094
num of homozygotes: 0

South Asian
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allele frequency: 1.302931596091205e-4
allele num: 15350
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.411e1

VQSLOD
type: SiteQuality
SIO_000300: 4.71e-1

FS
type: SiteQuality
SIO_000300: 6.786e0

BaseQRankSum
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SIO_000300: -3.055e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.78e-1

ClippingRankSum
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SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

DP
type: SiteQuality
SIO_000300: 1.336062e6

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.609114021819586e-5
allele num: 62146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16008
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.366e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.621e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

FS
type: SiteQuality
SIO_000300: 2.635e0

MQ
type: SiteQuality
SIO_000300: 5.873e1

DP
type: SiteQuality
SIO_000300: 1.421303e6

GenotypeQuality
all individuals: 1616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10968
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.588209135378947e-5
allele num: 62964
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 1.437263e6

FS
type: SiteQuality
SIO_000300: 1.122e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

QD
type: SiteQuality
SIO_000300: 1.073e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9574
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.588209135378947e-5
allele num: 62964
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10968
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 1.122e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.03e-1

QD
type: SiteQuality
SIO_000300: 1.073e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.437263e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64588
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.794365691727974e-4
allele num: 11146
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10018
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.54397233201581e-5
allele num: 64768
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.057e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

East Asian
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allele frequency: 1.184834123222749e-4
allele num: 8440
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66148
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
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MQRankSum
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FS
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DP
type: SiteQuality
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VQSLOD
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 437
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507295309296997e-5
allele num: 66344
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
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SIO_000300: 9.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

DP
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SIO_000300: 1.498961e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.353e0

FS
type: SiteQuality
SIO_000300: 2.692e0

QD
type: SiteQuality
SIO_000300: 1.255e1

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66344
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.351e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 8.699999999999999e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

DP
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SIO_000300: 1.499435e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.017e0

VQSLOD
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SIO_000300: 4.33e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505615947484116e-5
allele num: 66418
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.501573e6

VQSLOD
type: SiteQuality
SIO_000300: -2.526e0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 5.843e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.05e-1

FS
type: SiteQuality
SIO_000300: 4.072e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.301e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502900598154438e-5
allele num: 66538
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

FS
type: SiteQuality
SIO_000300: 9.218e0

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.506281e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.216e1

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.485e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.951e0

FS
type: SiteQuality
SIO_000300: 1.876e0

DP
type: SiteQuality
SIO_000300: 1.506462e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.171508903467666e-4
allele num: 8536
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.45e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

DP
type: SiteQuality
SIO_000300: 1.506694e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-3

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 9.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.911e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
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: 66552
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.648784253184099e-5
allele num: 10364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.04e-1

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

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.35e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.004988280545706e-5
allele num: 66556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.88e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.327e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 15

GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 904
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 15
allele frequency: 1.446759259259259e-3
allele num: 10368
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502855425308085e-5
allele num: 66540
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

VQSLOD
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MQ
type: SiteQuality
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QD
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ClippingRankSum
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MQRankSum
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SIO_000300: -1.98e-1

FS
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SIO_000300: 2.884e0

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.85e-1

GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

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

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

South Asian
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allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

InbreedingCoeff
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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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ClippingRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.50751e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 1.503171692270691e-5
allele num: 66526
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQ
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SIO_000300: 5.981e1

ClippingRankSum
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SIO_000300: -1.28e-1

FS
type: SiteQuality
SIO_000300: 6.264e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
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SIO_000300: 1.507406e6

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeQuality
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variant carriers: 2

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.515151515151515e-4
allele num: 6600
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503849855630414e-5
allele num: 66496
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.35e0

DP
type: SiteQuality
SIO_000300: 1.506661e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

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

QD
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SIO_000300: 1.331e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

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

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

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

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

Latino
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allele count: 2
allele frequency: 1.741250217656277e-4
allele num: 11486
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.39e-1

QD
type: SiteQuality
SIO_000300: 1.415e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.505551e6

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 5.24e0

VQSLOD
type: SiteQuality
SIO_000300: -1.958e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66426
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.911e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.7e-1

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

Latino
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allele count: 1
allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66388
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -3.0e-4

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

African
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allele count: 1
allele frequency: 9.765625000000001e-5
allele num: 10240
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66212
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
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allele count: 1
allele frequency: 8.753501400560224e-5
allele num: 11424
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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DP
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QD
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InbreedingCoeff
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BaseQRankSum
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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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Other
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.181474480151229e-4
allele num: 8464
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.865824782951855e-5
allele num: 10136
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 902
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66014
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.99e0

QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
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DP
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

MQ
type: SiteQuality
SIO_000300: 5.879e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.518833535844471e-5
allele num: 65840
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 16296
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10046
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.454075e6

BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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SIO_000300: -8.2e-1

ClippingRankSum
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SIO_000300: 5.22e-1

FS
type: SiteQuality
SIO_000300: 1.933e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.138e0

QD
type: SiteQuality
SIO_000300: 7.16e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8376
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Other
type: Population
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allele frequency: 0.0e0
allele num: 898
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Latino
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allele count: 1
allele frequency: 8.785802143735723e-5
allele num: 11382
num of homozygotes: 0

South Asian
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allele frequency: 6.148548942449582e-5
allele num: 16264
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65744
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -9.0e-4

MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
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SIO_000300: 1.440289e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.541402059313151e-5
allele num: 64876
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.857395925597875e-5
allele num: 11290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 7.253886010362695e-4
allele num: 9650
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.65e-2

DP
type: SiteQuality
SIO_000300: 1.423373e6

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

FS
type: SiteQuality
SIO_000300: 2.057e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

QD
type: SiteQuality
SIO_000300: 1.75e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65146
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10262
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 6.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.374883e6

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
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: 8622
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532191340054546e-5
allele num: 65266
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12980
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.95e-1

DP
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.48e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65288
num of homozygotes: 0

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

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

South Asian
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allele frequency: 7.59762953958365e-5
allele num: 13162
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

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

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

African
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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allele frequency: 1.478852410529429e-4
allele num: 13524
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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Other
type: Population
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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MQ
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FS
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InbreedingCoeff
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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African
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allele frequency: 1.938360147315371e-4
allele num: 10318
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65416
num of homozygotes: 0

East Asian
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South Asian
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VQSLOD
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ClippingRankSum
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DP
type: SiteQuality
SIO_000300: 2.397181e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.19e-1

QD
type: SiteQuality
SIO_000300: 1.335e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 5.984e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.617e0

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
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GenotypeQuality
all individuals: 930
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73190162798753e-4
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65452
num of homozygotes: 0

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

African
type: Population
allele count: 29
allele frequency: 2.811167119038387e-3
allele num: 10316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13610
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.14e0

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.73e-1

DP
type: SiteQuality
SIO_000300: 2.398075e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

QD
type: SiteQuality
SIO_000300: 1.204e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

GenotypeQuality
all individuals: 285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1285
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 459
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7363
bin: 9.75e1
variant carriers: 2019

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 112
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3286
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 99
bin: 4.25e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 117
allele frequency: 1.768974901723617e-2
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1737
allele frequency: 2.647220190197513e-2
allele num: 65616
num of homozygotes: 26

African
type: Population
allele count: 59
allele frequency: 5.704892670663314e-3
allele num: 10342
num of homozygotes: 1

South Asian
type: Population
allele count: 32
allele frequency: 2.290294875465216e-3
allele num: 13972
num of homozygotes: 0

Latino
type: Population
allele count: 98
allele frequency: 8.486317977138898e-3
allele num: 11548
num of homozygotes: 1

Other
type: Population
allele count: 14
allele frequency: 1.609195402298851e-2
allele num: 870
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.43e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

DP
type: SiteQuality
SIO_000300: 2.425888e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.408e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.18e0

GenotypeQuality
all individuals: 1314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2316
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 8473
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variant carriers: 0

GenotypeQuality
all individuals: 124
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variant carriers: 0

GenotypeQuality
all individuals: 34793
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variant carriers: 0

GenotypeQuality
all individuals: 549
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variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5555
bin: 9.75e1
variant carriers: 1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15930
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: 1
allele frequency: 1.508068164681044e-5
allele num: 66310
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.883e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.09e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 9.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.95e0

QD
type: SiteQuality
SIO_000300: 1.233e1

DP
type: SiteQuality
SIO_000300: 1.887695e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.22e-1

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3436
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 2319
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variant carriers: 0

GenotypeQuality
all individuals: 8509
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variant carriers: 0

GenotypeQuality
all individuals: 35291
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 950
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66462
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.161e1

DP
type: SiteQuality
SIO_000300: 1.893481e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

FS
type: SiteQuality
SIO_000300: 7.223e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.133e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

VQSLOD
type: SiteQuality
SIO_000300: 9.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.0e-1

GenotypeQuality
all individuals: 35424
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2317
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 3434
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 8514
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5556
bin: 9.75e1
variant carriers: 3

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: 3
allele frequency: 4.509786236132407e-5
allele num: 66522
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 16288
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.938e1

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

QD
type: SiteQuality
SIO_000300: 1.326e1

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.97e0

DP
type: SiteQuality
SIO_000300: 1.894925e6

FS
type: SiteQuality
SIO_000300: 5.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.93e-1

GenotypeQuality
all individuals: 155
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8523
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 949
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variant carriers: 0

GenotypeQuality
all individuals: 2658
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 3428
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
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: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.036e1

QD
type: SiteQuality
SIO_000300: 1.374e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

DP
type: SiteQuality
SIO_000300: 1.897456e6

GenotypeQuality
all individuals: 5552
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 35645
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 3427
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 949
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variant carriers: 0

GenotypeQuality
all individuals: 1312
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variant carriers: 0

GenotypeQuality
all individuals: 8538
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
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: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
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: 66614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.988e1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

VQSLOD
type: SiteQuality
SIO_000300: -9.172e-1

DP
type: SiteQuality
SIO_000300: 1.898525e6

QD
type: SiteQuality
SIO_000300: 1.424e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e0

FS
type: SiteQuality
SIO_000300: 4.013e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.195e0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 3418
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 2656
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variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 16504
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

FS
type: SiteQuality
SIO_000300: 1.293e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.715999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.679e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
type: SiteQuality
SIO_000300: 1.334e1

MQRankSum
type: SiteQuality
SIO_000300: -1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.123e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 1.899465e6

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 8559
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GenotypeQuality
all individuals: 1312
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35828
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999130252226854e-5
allele num: 66686
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: 8612
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.334e0

DP
type: SiteQuality
SIO_000300: 1.899299e6

VQSLOD
type: SiteQuality
SIO_000300: 7.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.895e0

MQRankSum
type: SiteQuality
SIO_000300: -7.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.87e-1

MQ
type: SiteQuality
SIO_000300: 5.99e1

QD
type: SiteQuality
SIO_000300: 1.366e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeQuality
all individuals: 2311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 2658
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
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variant carriers: 0

GenotypeQuality
all individuals: 5546
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variant carriers: 1

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35838
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 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: 8598
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: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
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: 6612
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.269e1

VQSLOD
type: SiteQuality
SIO_000300: 2.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e0

DP
type: SiteQuality
SIO_000300: 1.898951e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.64e-1

GenotypeQuality
all individuals: 2311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2658
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 8562
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998860433035446e-5
allele num: 66692
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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.898951e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

QD
type: SiteQuality
SIO_000300: 1.269e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e0

VQSLOD
type: SiteQuality
SIO_000300: 2.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

FS
type: SiteQuality
SIO_000300: 6.0e-1

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2311
bin: 8.25e1
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: 16510
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: 66712
num of homozygotes: 0

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

East Asian
type: Population
allele count: 8
allele frequency: 9.304489416143289e-4
allele num: 8598
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.044e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

QD
type: SiteQuality
SIO_000300: 1.693e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

DP
type: SiteQuality
SIO_000300: 1.898493e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 950
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variant carriers: 0

GenotypeQuality
all individuals: 8557
bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49734656552634e-5
allele num: 66706
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.89705e6

FS
type: SiteQuality
SIO_000300: 1.835e0

QD
type: SiteQuality
SIO_000300: 1.354e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
all individuals: 35857
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2655
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 3427
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

DP
type: SiteQuality
SIO_000300: 1.89705e6

QD
type: SiteQuality
SIO_000300: 1.354e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.36e-1

FS
type: SiteQuality
SIO_000300: 1.835e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

GenotypeQuality
all individuals: 950
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35860
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variant carriers: 0

GenotypeQuality
all individuals: 2654
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8555
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5531
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

VQSLOD
type: SiteQuality
SIO_000300: 3.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 5.911e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.692e0

DP
type: SiteQuality
SIO_000300: 1.896341e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.371e1

GenotypeQuality
all individuals: 1313
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
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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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3421
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

QD
type: SiteQuality
SIO_000300: 1.459e1

VQSLOD
type: SiteQuality
SIO_000300: 4.03e0

DP
type: SiteQuality
SIO_000300: 1.89567e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

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

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 16510
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.508e-1

QD
type: SiteQuality
SIO_000300: 1.541e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

DP
type: SiteQuality
SIO_000300: 1.895421e6

FS
type: SiteQuality
SIO_000300: 6.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

MQ
type: SiteQuality
SIO_000300: 5.871e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.213e0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.895128e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.157e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.788e0

VQSLOD
type: SiteQuality
SIO_000300: -3.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.513e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2310
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5525
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35890
bin: 6.25e1
variant carriers: 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: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.894872e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
SIO_000300: 1.375e1

FS
type: SiteQuality
SIO_000300: 4.77e0

VQSLOD
type: SiteQuality
SIO_000300: 4.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.710000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeQuality
all individuals: 946
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1312
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2654
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3415
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 8.374000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: -5.489000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

DP
type: SiteQuality
SIO_000300: 1.894643e6

QD
type: SiteQuality
SIO_000300: 1.306e1

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

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

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

GenotypeQuality
all individuals: 35884
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2656
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5521
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8564
bin: 6.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.140000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

QD
type: SiteQuality
SIO_000300: 1.396e1

MQ
type: SiteQuality
SIO_000300: 5.989e1

MQRankSum
type: SiteQuality
SIO_000300: -3.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.206e0

DP
type: SiteQuality
SIO_000300: 1.894388e6

GenotypeQuality
all individuals: 3417
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1310
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35884
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2656
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8564
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5521
bin: 9.75e1
variant carriers: 3

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: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997332374186974e-5
allele num: 66726
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.140000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.894388e6

MQRankSum
type: SiteQuality
SIO_000300: -3.89e-1

QD
type: SiteQuality
SIO_000300: 1.396e1

MQ
type: SiteQuality
SIO_000300: 5.989e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.206e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 947
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3415
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5519
bin: 9.75e1
variant carriers: 5

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

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

GenotypeQuality
all individuals: 8559
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35886
bin: 6.25e1
variant carriers: 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: 16510
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.804920238324044e-4
allele num: 10406
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: 0
allele frequency: 0.0e0
allele num: 66728
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: 8596
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.9e0

QD
type: SiteQuality
SIO_000300: 1.451e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.893629e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.392e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.73e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1