21-30934101-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934101
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934101
    reference: chr 21
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35789T>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2206A>G
  hgvsp: ENSP00000446326.1:p.Arg736Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2200A>G
  hgvsp: ENSP00000373776.2:p.Arg734Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2200A>G
  hgvsp: ENSP00000382797.1:p.Arg734Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2200A>G
  hgvsp: ENSP00000327687.4:p.Arg734Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2200A>G
  hgvsp: ENSP00000382791.1:p.Arg734Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2155A>G
  hgvsp: ENSP00000382793.1:p.Arg719Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2155A>G
  hgvsp: ENSP00000373777.3:p.Arg719Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2155A>G
  hgvsp: ENSP00000382798.1:p.Arg719Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20531T>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2206A>G
  hgvsp: ENSP00000311646.7:p.Arg736Gly
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg734Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

21-30934106-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934106
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934106
    reference: chr 21
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2195T>C
  hgvsp: ENSP00000373776.2:p.Leu732Pro
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2201T>C
  hgvsp: ENSP00000311646.7:p.Leu734Pro
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2150T>C
  hgvsp: ENSP00000373777.3:p.Leu717Pro
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2150T>C
  hgvsp: ENSP00000382798.1:p.Leu717Pro
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2195T>C
  hgvsp: ENSP00000327687.4:p.Leu732Pro
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2195T>C
  hgvsp: ENSP00000382791.1:p.Leu732Pro
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2150T>C
  hgvsp: ENSP00000382793.1:p.Leu717Pro
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2195T>C
  hgvsp: ENSP00000382797.1:p.Leu732Pro
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20526A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2201T>C
  hgvsp: ENSP00000446326.1:p.Leu734Pro
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35784A>G
  variant of: http://identifiers.org/hgnc/935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu732Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

21-30934110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934110
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934110
    reference: chr 21
allele count: 20
allele frequency: 1.653548515113433e-4
allele num: 120952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2146G>A
  hgvsp: ENSP00000382793.1:p.Ala716Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2197G>A
  hgvsp: ENSP00000311646.7:p.Ala733Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2191G>A
  hgvsp: ENSP00000373776.2:p.Ala731Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2191G>A
  hgvsp: ENSP00000327687.4:p.Ala731Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35780C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2146G>A
  hgvsp: ENSP00000373777.3:p.Ala716Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2146G>A
  hgvsp: ENSP00000382798.1:p.Ala716Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20522C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2191G>A
  hgvsp: ENSP00000382797.1:p.Ala731Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2191G>A
  hgvsp: ENSP00000382791.1:p.Ala731Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2197G>A
  hgvsp: ENSP00000446326.1:p.Ala733Thr
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32110
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala731Thr
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

21-30934111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934111
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934111
    reference: chr 21
allele count: 2
allele frequency: 1.65371258475277e-5
allele num: 120940
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35779G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2190C>T
  hgvsp: ENST00000399913.1:c.2190C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2145C>T
  hgvsp: ENST00000399914.1:c.2145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2196C>T
  hgvsp: ENST00000309434.7:c.2196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2190C>T
  hgvsp: ENST00000327783.4:c.2190C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20521G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2190C>T
  hgvsp: ENST00000389124.2:c.2190C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2145C>T
  hgvsp: ENST00000399909.1:c.2145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2190C>T
  hgvsp: ENST00000399907.1:c.2190C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2145C>T
  hgvsp: ENST00000389125.3:c.2145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2196C>T
  hgvsp: ENST00000535441.1:c.2196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr730Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

21-30934114-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934114
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934114
    reference: chr 21
allele count: 1
allele frequency: 8.29228651508367e-6
allele num: 120594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2187G>A
  hgvsp: ENST00000389124.2:c.2187G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2142G>A
  hgvsp: ENST00000399914.1:c.2142G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2193G>A
  hgvsp: ENST00000535441.1:c.2193G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2187G>A
  hgvsp: ENST00000399907.1:c.2187G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2187G>A
  hgvsp: ENST00000399913.1:c.2187G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35776C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20518C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2142G>A
  hgvsp: ENST00000389125.3:c.2142G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2187G>A
  hgvsp: ENST00000327783.4:c.2187G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2142G>A
  hgvsp: ENST00000399909.1:c.2142G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2193G>A
  hgvsp: ENST00000309434.7:c.2193G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln729Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

21-30934121-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934121
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934121
    reference: chr 21
allele count: 1
allele frequency: 8.305233958440609e-6
allele num: 120406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2135G>A
  hgvsp: ENSP00000382793.1:p.Arg712Lys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2135G>A
  hgvsp: ENSP00000382798.1:p.Arg712Lys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2135G>A
  hgvsp: ENSP00000373777.3:p.Arg712Lys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2186G>A
  hgvsp: ENSP00000311646.7:p.Arg729Lys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2180G>A
  hgvsp: ENSP00000327687.4:p.Arg727Lys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2180G>A
  hgvsp: ENSP00000382797.1:p.Arg727Lys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35769C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2186G>A
  hgvsp: ENSP00000446326.1:p.Arg729Lys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2180G>A
  hgvsp: ENSP00000373776.2:p.Arg727Lys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2180G>A
  hgvsp: ENSP00000382791.1:p.Arg727Lys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20511C>T
  variant of: http://identifiers.org/hgnc/935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg727Lys
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

21-30934130-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934130
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934130
    reference: chr 21
allele count: 1
allele frequency: 8.379560575843403e-6
allele num: 119338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2177T>C
  hgvsp: ENSP00000446326.1:p.Met726Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2126T>C
  hgvsp: ENSP00000373777.3:p.Met709Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2171T>C
  hgvsp: ENSP00000373776.2:p.Met724Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2177T>C
  hgvsp: ENSP00000311646.7:p.Met726Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2126T>C
  hgvsp: ENSP00000382798.1:p.Met709Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2171T>C
  hgvsp: ENSP00000382791.1:p.Met724Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2171T>C
  hgvsp: ENSP00000327687.4:p.Met724Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20502A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35760A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2171T>C
  hgvsp: ENSP00000382797.1:p.Met724Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2126T>C
  hgvsp: ENSP00000382793.1:p.Met709Thr
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met724Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

21-30934137-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934137
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934137
    reference: chr 21
allele count: 1
allele frequency: 8.495887990212738e-6
allele num: 117704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2164G>A
  hgvsp: ENSP00000327687.4:p.Ala722Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2164G>A
  hgvsp: ENSP00000373776.2:p.Ala722Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2119G>A
  hgvsp: ENSP00000382793.1:p.Ala707Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2164G>A
  hgvsp: ENSP00000382791.1:p.Ala722Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20495C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2164G>A
  hgvsp: ENSP00000382797.1:p.Ala722Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2170G>A
  hgvsp: ENSP00000446326.1:p.Ala724Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2170G>A
  hgvsp: ENSP00000311646.7:p.Ala724Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35753C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2119G>A
  hgvsp: ENSP00000373777.3:p.Ala707Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2119G>A
  hgvsp: ENSP00000382798.1:p.Ala707Thr
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala722Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum

21-30934140-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934140
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934140
    reference: chr 21
allele count: 3
allele frequency: 2.5790478155465e-5
allele num: 116322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2161T>A
  hgvsp: ENSP00000327687.4:p.Trp721Arg
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2161T>A
  hgvsp: ENSP00000382797.1:p.Trp721Arg
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2161T>A
  hgvsp: ENSP00000382791.1:p.Trp721Arg
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2167T>A
  hgvsp: ENSP00000311646.7:p.Trp723Arg
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2161T>A
  hgvsp: ENSP00000373776.2:p.Trp721Arg
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2167T>A
  hgvsp: ENSP00000446326.1:p.Trp723Arg
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2116T>A
  hgvsp: ENSP00000382793.1:p.Trp706Arg
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2116T>A
  hgvsp: ENSP00000373777.3:p.Trp706Arg
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2116T>A
  hgvsp: ENSP00000382798.1:p.Trp706Arg
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35750A>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20492A>T
  variant of: http://identifiers.org/hgnc/935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp721Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

21-30934146-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934146
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934146
    reference: chr 21
allele count: 1
allele frequency: 8.789354334030623e-6
allele num: 113774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20486T>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2155A>G
  hgvsp: ENSP00000373776.2:p.Lys719Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2155A>G
  hgvsp: ENSP00000382791.1:p.Lys719Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2110A>G
  hgvsp: ENSP00000382793.1:p.Lys704Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2161A>G
  hgvsp: ENSP00000311646.7:p.Lys721Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2155A>G
  hgvsp: ENSP00000327687.4:p.Lys719Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2110A>G
  hgvsp: ENSP00000382798.1:p.Lys704Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2161A>G
  hgvsp: ENSP00000446326.1:p.Lys721Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2110A>G
  hgvsp: ENSP00000373777.3:p.Lys704Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35744T>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2155A>G
  hgvsp: ENSP00000382797.1:p.Lys719Glu
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys719Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

21-30934151-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934151
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934151
    reference: chr 21
allele count: 1
allele frequency: 9.068156262468716e-6
allele num: 110276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20481T>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35739T>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2105A>G
  hgvsp: ENSP00000382798.1:p.Tyr702Cys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2150A>G
  hgvsp: ENSP00000382797.1:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2150A>G
  hgvsp: ENSP00000327687.4:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2105A>G
  hgvsp: ENSP00000373777.3:p.Tyr702Cys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2156A>G
  hgvsp: ENSP00000311646.7:p.Tyr719Cys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2150A>G
  hgvsp: ENSP00000382791.1:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2150A>G
  hgvsp: ENSP00000373776.2:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2105A>G
  hgvsp: ENSP00000382793.1:p.Tyr702Cys
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2156A>G
  hgvsp: ENSP00000446326.1:p.Tyr719Cys
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr717Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

21-30934152-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934152
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934152
    reference: chr 21
allele count: 1
allele frequency: 9.069307649054072e-6
allele num: 110262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35738A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2155T>C
  hgvsp: ENSP00000311646.7:p.Tyr719His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2104T>C
  hgvsp: ENSP00000382793.1:p.Tyr702His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2149T>C
  hgvsp: ENSP00000382791.1:p.Tyr717His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2155T>C
  hgvsp: ENSP00000446326.1:p.Tyr719His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2149T>C
  hgvsp: ENSP00000327687.4:p.Tyr717His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2104T>C
  hgvsp: ENSP00000373777.3:p.Tyr702His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20480A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2104T>C
  hgvsp: ENSP00000382798.1:p.Tyr702His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2149T>C
  hgvsp: ENSP00000373776.2:p.Tyr717His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2149T>C
  hgvsp: ENSP00000382797.1:p.Tyr717His
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr717His
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

21-30934153-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934153
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934153
    reference: chr 21
allele count: 5
allele frequency: 4.561045026636503e-5
allele num: 109624
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20479G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2148C>T
  hgvsp: ENST00000399907.1:c.2148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2103C>T
  hgvsp: ENST00000399909.1:c.2103C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2148C>T
  hgvsp: ENST00000389124.2:c.2148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2148C>T
  hgvsp: ENST00000327783.4:c.2148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2103C>T
  hgvsp: ENST00000399914.1:c.2103C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2154C>T
  hgvsp: ENST00000535441.1:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2103C>T
  hgvsp: ENST00000389125.3:c.2103C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35737G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2154C>T
  hgvsp: ENST00000309434.7:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2148C>T
  hgvsp: ENST00000399913.1:c.2148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr716Thr
num of homozygotes: 1
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

21-30934154-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934154
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934154
    reference: chr 21
allele count: 1
allele frequency: 9.183242419233382e-6
allele num: 108894
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2147C>T
  hgvsp: ENSP00000382791.1:p.Thr716Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35736G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2102C>T
  hgvsp: ENSP00000373777.3:p.Thr701Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2147C>T
  hgvsp: ENSP00000382797.1:p.Thr716Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2147C>T
  hgvsp: ENSP00000373776.2:p.Thr716Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20478G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2153C>T
  hgvsp: ENSP00000311646.7:p.Thr718Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2147C>T
  hgvsp: ENSP00000327687.4:p.Thr716Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2102C>T
  hgvsp: ENSP00000382798.1:p.Thr701Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2102C>T
  hgvsp: ENSP00000382793.1:p.Thr701Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2153C>T
  hgvsp: ENSP00000446326.1:p.Thr718Ile
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr716Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

21-30934155-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934155
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934154
    reference: chr 21
allele count: 1
allele frequency: 9.391258616479781e-6
allele num: 106482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2145delC
  hgvsp: ENSP00000327687.4:p.Thr716ProfsTer9
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2145delC
  hgvsp: ENSP00000382797.1:p.Thr716ProfsTer9
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2151delC
  hgvsp: ENSP00000311646.7:p.Thr718ProfsTer9
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2145delC
  hgvsp: ENSP00000373776.2:p.Thr716ProfsTer9
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2151delC
  hgvsp: ENSP00000446326.1:p.Thr718ProfsTer9
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2145delC
  hgvsp: ENSP00000382791.1:p.Thr716ProfsTer9
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2100delC
  hgvsp: ENSP00000373777.3:p.Thr701ProfsTer9
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2100delC
  hgvsp: ENSP00000382798.1:p.Thr701ProfsTer9
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20475delG
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35733delG
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2100delC
  hgvsp: ENSP00000382793.1:p.Thr701ProfsTer9
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20410
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr716ProfsTer9
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: TG
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

21-30934166-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934166
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934166
    reference: chr 21
allele count: 1
allele frequency: 1.019742209169522e-5
allele num: 98064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2135C>A
  hgvsp: ENSP00000327687.4:p.Ser712Ter
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2135C>A
  hgvsp: ENSP00000373776.2:p.Ser712Ter
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20466G>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2135C>A
  hgvsp: ENSP00000382791.1:p.Ser712Ter
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2141C>A
  hgvsp: ENSP00000446326.1:p.Ser714Ter
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35724G>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2090C>A
  hgvsp: ENSP00000373777.3:p.Ser697Ter
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2141C>A
  hgvsp: ENSP00000311646.7:p.Ser714Ter
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2090C>A
  hgvsp: ENSP00000382793.1:p.Ser697Ter
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2090C>A
  hgvsp: ENSP00000382798.1:p.Ser697Ter
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2135C>A
  hgvsp: ENSP00000382797.1:p.Ser712Ter
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14561
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14599
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser712Ter
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

21-30934173-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934173
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934173
    reference: chr 21
allele count: 4
allele frequency: 4.318068959561284e-5
allele num: 92634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35717G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2137-3C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20459G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2086-3C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2137-3C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2086-3C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2131-3C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2131-3C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2131-3C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2086-3C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2131-3C>T
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18077
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2131-3C>T
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

21-30934183-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934183
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934183
    reference: chr 21
allele count: 1
allele frequency: 1.16544683231551e-5
allele num: 85804
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20449A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2086-13T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2131-13T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2137-13T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2086-13T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2131-13T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2131-13T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2086-13T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2137-13T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2131-13T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35707A>G
  variant of: http://identifiers.org/hgnc/935
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21583
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3630
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/21-30934200-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934200
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934200
    reference: chr 21
allele count: 1
allele frequency: 1.432623707057104e-5
allele num: 69802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20432A>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2131-30T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2086-30T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35690A>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2086-30T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2086-30T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2131-30T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2131-30T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2131-30T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2137-30T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2137-30T>G
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5917
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20626
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

21-30934204-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934204
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934204
    reference: chr 21
allele count: 1
allele frequency: 1.511487303506651e-5
allele num: 66160
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2131-34C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2137-34C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2086-34C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2131-34C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35686G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2086-34C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2086-34C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2131-34C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2131-34C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20428G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2137-34C>T
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

21-30934220-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934220
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934220
    reference: chr 21
allele count: 11
allele frequency: 2.11522190600723e-4
allele num: 52004
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2131-50G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2131-50G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2131-50G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2137-50G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2086-50G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2086-50G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2131-50G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35670C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2086-50G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20412C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2137-50G>A
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13532
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25379
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7773
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3836
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8475
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

21-30934221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30934221
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30934221
    reference: chr 21
allele count: 0
allele frequency: 0.0e0
allele num: 51452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-20411G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-35669G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2086-51C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2131-51C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2137-51C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2086-51C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2131-51C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2137-51C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2131-51C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2131-51C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2086-51C>T
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 7794
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25512
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS

21-30949246-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949246
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949246
    reference: chr 21
allele count: 1
allele frequency: 8.459091831900928e-6
allele num: 118216
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2136+38T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2136+38T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5386A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2130+38T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2085+38T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2085+38T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2130+38T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2085+38T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20644A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2130+38T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2130+38T>C
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2623
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

21-30949257-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949257
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949257
    reference: chr 21
allele count: 3
allele frequency: 2.527422534499318e-5
allele num: 118698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2130+27T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2085+27T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2130+27T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20633A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2130+27T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2130+27T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2085+27T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2085+27T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2136+27T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5375A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2136+27T>C
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9246
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

21-30949266-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949266
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949266
    reference: chr 21
allele count: 1
allele frequency: 8.384619254439656e-6
allele num: 119266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2136+18T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2136+18T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2130+18T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2085+18T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2085+18T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2130+18T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5366A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2130+18T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2085+18T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20624A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2130+18T>C
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

21-30949267-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949267
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949267
    reference: chr 21
allele count: 6
allele frequency: 5.031362157448093e-5
allele num: 119252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2085+17G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2130+17G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2085+17G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2085+17G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2130+17G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5365C>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2136+17G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20623C>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2130+17G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2136+17G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2130+17G>C
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5218
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

21-30949267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949267
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949267
    reference: chr 21
allele count: 1
allele frequency: 8.385603595746822e-6
allele num: 119252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2085+17G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2130+17G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20623C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2130+17G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2130+17G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5365C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2136+17G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2085+17G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2130+17G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2136+17G>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2085+17G>A
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3021
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

21-30949270-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949270
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949270
    reference: chr 21
allele count: 1
allele frequency: 8.370862701109976e-6
allele num: 119462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2085+14A>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2130+14A>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2130+14A>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2130+14A>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2136+14A>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2085+14A>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20620T>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2136+14A>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5362T>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2130+14A>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2085+14A>G
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12818
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

21-30949271-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949271
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949271
    reference: chr 21
allele count: 2
allele frequency: 1.673500125512509e-5
allele num: 119510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2085+13C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2136+13C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2085+13C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2130+13C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2085+13C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5361G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2130+13C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2130+13C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2136+13C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20619G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2130+13C>T
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

21-30949271-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949271
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949271
    reference: chr 21
allele count: 1
allele frequency: 8.367500627562547e-6
allele num: 119510
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2130+13C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20619G>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2130+13C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2130+13C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2085+13C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2130+13C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2085+13C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5361G>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2085+13C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2136+13C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2136+13C>G
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2646
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

21-30949275-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949275
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949275
    reference: chr 21
allele count: 1
allele frequency: 8.347384764353328e-6
allele num: 119798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2085+9C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2130+9C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5357G>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20615G>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2136+9C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2130+9C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2130+9C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2085+9C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2085+9C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2136+9C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2130+9C>A
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/21-30949296-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949296
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949296
    reference: chr 21
allele count: 3
allele frequency: 2.481430627471092e-5
allele num: 120898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2073G>T
  hgvsp: ENSP00000382798.1:p.Met691Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2118G>T
  hgvsp: ENSP00000382797.1:p.Met706Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2118G>T
  hgvsp: ENSP00000373776.2:p.Met706Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2118G>T
  hgvsp: ENSP00000327687.4:p.Met706Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2124G>T
  hgvsp: ENSP00000311646.7:p.Met708Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2073G>T
  hgvsp: ENSP00000382793.1:p.Met691Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2118G>T
  hgvsp: ENSP00000382791.1:p.Met706Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2073G>T
  hgvsp: ENSP00000373777.3:p.Met691Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5336C>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20594C>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2124G>T
  hgvsp: ENSP00000446326.1:p.Met708Ile
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Met706Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

21-30949300-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949300
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949300
    reference: chr 21
allele count: 1
allele frequency: 8.262414277451872e-6
allele num: 121030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2069C>T
  hgvsp: ENSP00000382798.1:p.Thr690Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2114C>T
  hgvsp: ENSP00000382797.1:p.Thr705Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2120C>T
  hgvsp: ENSP00000446326.1:p.Thr707Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2069C>T
  hgvsp: ENSP00000382793.1:p.Thr690Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2114C>T
  hgvsp: ENSP00000327687.4:p.Thr705Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2120C>T
  hgvsp: ENSP00000311646.7:p.Thr707Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5332G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2069C>T
  hgvsp: ENSP00000373777.3:p.Thr690Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2114C>T
  hgvsp: ENSP00000382791.1:p.Thr705Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20590G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2114C>T
  hgvsp: ENSP00000373776.2:p.Thr705Ile
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr705Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

21-30949303-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949303
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949303
    reference: chr 21
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2066C>T
  hgvsp: ENSP00000382798.1:p.Ser689Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2117C>T
  hgvsp: ENSP00000311646.7:p.Ser706Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2111C>T
  hgvsp: ENSP00000327687.4:p.Ser704Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2117C>T
  hgvsp: ENSP00000446326.1:p.Ser706Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5329G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2111C>T
  hgvsp: ENSP00000382791.1:p.Ser704Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20587G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2111C>T
  hgvsp: ENSP00000382797.1:p.Ser704Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2066C>T
  hgvsp: ENSP00000373777.3:p.Ser689Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2066C>T
  hgvsp: ENSP00000382793.1:p.Ser689Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2111C>T
  hgvsp: ENSP00000373776.2:p.Ser704Leu
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser704Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

21-30949308-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949308
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949308
    reference: chr 21
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2112T>C
  hgvsp: ENST00000309434.7:c.2112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2106T>C
  hgvsp: ENST00000327783.4:c.2106T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2106T>C
  hgvsp: ENST00000399913.1:c.2106T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2106T>C
  hgvsp: ENST00000399907.1:c.2106T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2061T>C
  hgvsp: ENST00000399909.1:c.2061T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2112T>C
  hgvsp: ENST00000535441.1:c.2112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2106T>C
  hgvsp: ENST00000389124.2:c.2106T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2061T>C
  hgvsp: ENST00000389125.3:c.2061T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20582A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2061T>C
  hgvsp: ENST00000399914.1:c.2061T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5324A>G
  variant of: http://identifiers.org/hgnc/935
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp702Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

21-30949308-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949308
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949308
    reference: chr 21
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2106T>A
  hgvsp: ENSP00000373776.2:p.Asp702Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2061T>A
  hgvsp: ENSP00000382793.1:p.Asp687Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2112T>A
  hgvsp: ENSP00000446326.1:p.Asp704Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2106T>A
  hgvsp: ENSP00000382797.1:p.Asp702Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2061T>A
  hgvsp: ENSP00000373777.3:p.Asp687Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2112T>A
  hgvsp: ENSP00000311646.7:p.Asp704Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20582A>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5324A>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2061T>A
  hgvsp: ENSP00000382798.1:p.Asp687Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2106T>A
  hgvsp: ENSP00000382791.1:p.Asp702Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2106T>A
  hgvsp: ENSP00000327687.4:p.Asp702Glu
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp702Glu
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

21-30949315-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949315
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949315
    reference: chr 21
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2054T>C
  hgvsp: ENSP00000373777.3:p.Val685Ala
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2054T>C
  hgvsp: ENSP00000382798.1:p.Val685Ala
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2105T>C
  hgvsp: ENSP00000446326.1:p.Val702Ala
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20575A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2099T>C
  hgvsp: ENSP00000373776.2:p.Val700Ala
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2099T>C
  hgvsp: ENSP00000327687.4:p.Val700Ala
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2105T>C
  hgvsp: ENSP00000311646.7:p.Val702Ala
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2054T>C
  hgvsp: ENSP00000382793.1:p.Val685Ala
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2099T>C
  hgvsp: ENSP00000382791.1:p.Val700Ala
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5317A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2099T>C
  hgvsp: ENSP00000382797.1:p.Val700Ala
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val700Ala
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/21-30949316-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949316
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949316
    reference: chr 21
allele count: 12
allele frequency: 9.891522964819151e-5
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2104G>T
  hgvsp: ENSP00000311646.7:p.Val702Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2053G>T
  hgvsp: ENSP00000382798.1:p.Val685Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5316C>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2053G>T
  hgvsp: ENSP00000373777.3:p.Val685Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2053G>T
  hgvsp: ENSP00000382793.1:p.Val685Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2104G>T
  hgvsp: ENSP00000446326.1:p.Val702Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2098G>T
  hgvsp: ENSP00000373776.2:p.Val700Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2098G>T
  hgvsp: ENSP00000327687.4:p.Val700Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2098G>T
  hgvsp: ENSP00000382797.1:p.Val700Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2098G>T
  hgvsp: ENSP00000382791.1:p.Val700Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20574C>A
  variant of: http://identifiers.org/hgnc/935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val700Phe
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

21-30949317-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949317
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949317
    reference: chr 21
allele count: 8
allele frequency: 6.594239931419904e-5
allele num: 121318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2052G>A
  hgvsp: ENST00000399909.1:c.2052G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2097G>A
  hgvsp: ENST00000327783.4:c.2097G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2103G>A
  hgvsp: ENST00000535441.1:c.2103G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2052G>A
  hgvsp: ENST00000389125.3:c.2052G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2097G>A
  hgvsp: ENST00000399913.1:c.2097G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2052G>A
  hgvsp: ENST00000399914.1:c.2052G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5315C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2097G>A
  hgvsp: ENST00000389124.2:c.2097G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2103G>A
  hgvsp: ENST00000309434.7:c.2103G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20573C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2097G>A
  hgvsp: ENST00000399907.1:c.2097G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 11563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala699Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

21-30949318-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949318
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949318
    reference: chr 21
allele count: 2
allele frequency: 1.648451280022419e-5
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2096C>T
  hgvsp: ENSP00000382791.1:p.Ala699Val
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2051C>T
  hgvsp: ENSP00000382798.1:p.Ala684Val
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2096C>T
  hgvsp: ENSP00000373776.2:p.Ala699Val
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20572G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2051C>T
  hgvsp: ENSP00000373777.3:p.Ala684Val
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2096C>T
  hgvsp: ENSP00000327687.4:p.Ala699Val
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5314G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2096C>T
  hgvsp: ENSP00000382797.1:p.Ala699Val
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2102C>T
  hgvsp: ENSP00000446326.1:p.Ala701Val
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2051C>T
  hgvsp: ENSP00000382793.1:p.Ala684Val
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2102C>T
  hgvsp: ENSP00000311646.7:p.Ala701Val
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala699Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

21-30949318-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949318
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949318
    reference: chr 21
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2102C>G
  hgvsp: ENSP00000446326.1:p.Ala701Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2051C>G
  hgvsp: ENSP00000373777.3:p.Ala684Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2102C>G
  hgvsp: ENSP00000311646.7:p.Ala701Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2096C>G
  hgvsp: ENSP00000327687.4:p.Ala699Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2096C>G
  hgvsp: ENSP00000373776.2:p.Ala699Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20572G>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2096C>G
  hgvsp: ENSP00000382791.1:p.Ala699Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2051C>G
  hgvsp: ENSP00000382798.1:p.Ala684Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5314G>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2051C>G
  hgvsp: ENSP00000382793.1:p.Ala684Gly
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2096C>G
  hgvsp: ENSP00000382797.1:p.Ala699Gly
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala699Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

21-30949323-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949323
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949323
    reference: chr 21
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20567A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5309A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2091T>C
  hgvsp: ENST00000399907.1:c.2091T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2091T>C
  hgvsp: ENST00000399913.1:c.2091T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2046T>C
  hgvsp: ENST00000399909.1:c.2046T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2091T>C
  hgvsp: ENST00000389124.2:c.2091T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2046T>C
  hgvsp: ENST00000389125.3:c.2046T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2097T>C
  hgvsp: ENST00000535441.1:c.2097T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2097T>C
  hgvsp: ENST00000309434.7:c.2097T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2091T>C
  hgvsp: ENST00000327783.4:c.2091T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2046T>C
  hgvsp: ENST00000399914.1:c.2046T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr697Tyr
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

21-30949325-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949325
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949325
    reference: chr 21
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2044T>C
  hgvsp: ENSP00000373777.3:p.Tyr682His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2089T>C
  hgvsp: ENSP00000382797.1:p.Tyr697His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2089T>C
  hgvsp: ENSP00000327687.4:p.Tyr697His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2044T>C
  hgvsp: ENSP00000382798.1:p.Tyr682His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2095T>C
  hgvsp: ENSP00000311646.7:p.Tyr699His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2089T>C
  hgvsp: ENSP00000382791.1:p.Tyr697His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2044T>C
  hgvsp: ENSP00000382793.1:p.Tyr682His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5307A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2089T>C
  hgvsp: ENSP00000373776.2:p.Tyr697His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2095T>C
  hgvsp: ENSP00000446326.1:p.Tyr699His
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20565A>G
  variant of: http://identifiers.org/hgnc/935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr697His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

21-30949341-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949341
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949341
    reference: chr 21
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2028G>A
  hgvsp: ENST00000389125.3:c.2028G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2028G>A
  hgvsp: ENST00000399909.1:c.2028G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5291C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2073G>A
  hgvsp: ENST00000389124.2:c.2073G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2073G>A
  hgvsp: ENST00000327783.4:c.2073G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2073G>A
  hgvsp: ENST00000399907.1:c.2073G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2079G>A
  hgvsp: ENST00000309434.7:c.2079G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20549C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2073G>A
  hgvsp: ENST00000399913.1:c.2073G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2028G>A
  hgvsp: ENST00000399914.1:c.2028G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2079G>A
  hgvsp: ENST00000535441.1:c.2079G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys691Lys
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

21-30949359-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949359
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949359
    reference: chr 21
allele count: 6
allele frequency: 4.942420797706717e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2055G>A
  hgvsp: ENST00000399913.1:c.2055G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2055G>A
  hgvsp: ENST00000327783.4:c.2055G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2061G>A
  hgvsp: ENST00000309434.7:c.2061G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2055G>A
  hgvsp: ENST00000399907.1:c.2055G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2055G>A
  hgvsp: ENST00000389124.2:c.2055G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2010G>A
  hgvsp: ENST00000399909.1:c.2010G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2010G>A
  hgvsp: ENST00000389125.3:c.2010G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2010G>A
  hgvsp: ENST00000399914.1:c.2010G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20531C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5273C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2061G>A
  hgvsp: ENST00000535441.1:c.2061G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ser685Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

21-30949359-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949359
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949358
    reference: chr 21
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2009delC
  hgvsp: ENSP00000382793.1:p.Ser670TrpfsTer11
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2054delC
  hgvsp: ENSP00000327687.4:p.Ser685TrpfsTer11
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2060delC
  hgvsp: ENSP00000311646.7:p.Ser687TrpfsTer11
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2009delC
  hgvsp: ENSP00000382798.1:p.Ser670TrpfsTer11
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2054delC
  hgvsp: ENSP00000382797.1:p.Ser685TrpfsTer11
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2009delC
  hgvsp: ENSP00000373777.3:p.Ser670TrpfsTer11
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2054delC
  hgvsp: ENSP00000373776.2:p.Ser685TrpfsTer11
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20530delG
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5272delG
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2054delC
  hgvsp: ENSP00000382791.1:p.Ser685TrpfsTer11
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2060delC
  hgvsp: ENSP00000446326.1:p.Ser687TrpfsTer11
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser685TrpfsTer11
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: CG
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

21-30949360-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949360
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949360
    reference: chr 21
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2054C>T
  hgvsp: ENSP00000382797.1:p.Ser685Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2054C>T
  hgvsp: ENSP00000382791.1:p.Ser685Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5272G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2060C>T
  hgvsp: ENSP00000446326.1:p.Ser687Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2054C>T
  hgvsp: ENSP00000327687.4:p.Ser685Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20530G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2009C>T
  hgvsp: ENSP00000373777.3:p.Ser670Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2060C>T
  hgvsp: ENSP00000311646.7:p.Ser687Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2009C>T
  hgvsp: ENSP00000382798.1:p.Ser670Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2009C>T
  hgvsp: ENSP00000382793.1:p.Ser670Leu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2054C>T
  hgvsp: ENSP00000373776.2:p.Ser685Leu
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser685Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

21-30949366-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949366
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949366
    reference: chr 21
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20524A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.2003T>C
  hgvsp: ENSP00000382793.1:p.Ile668Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2054T>C
  hgvsp: ENSP00000311646.7:p.Ile685Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2048T>C
  hgvsp: ENSP00000382791.1:p.Ile683Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5266A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.2003T>C
  hgvsp: ENSP00000382798.1:p.Ile668Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2048T>C
  hgvsp: ENSP00000373776.2:p.Ile683Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2054T>C
  hgvsp: ENSP00000446326.1:p.Ile685Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2048T>C
  hgvsp: ENSP00000327687.4:p.Ile683Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.2003T>C
  hgvsp: ENSP00000373777.3:p.Ile668Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2048T>C
  hgvsp: ENSP00000382797.1:p.Ile683Thr
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11578
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile683Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

21-30949372-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949372
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949372
    reference: chr 21
allele count: 6
allele frequency: 4.942095118857387e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2042C>T
  hgvsp: ENSP00000382797.1:p.Ser681Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2042C>T
  hgvsp: ENSP00000327687.4:p.Ser681Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2048C>T
  hgvsp: ENSP00000311646.7:p.Ser683Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1997C>T
  hgvsp: ENSP00000382793.1:p.Ser666Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2042C>T
  hgvsp: ENSP00000373776.2:p.Ser681Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20518G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2042C>T
  hgvsp: ENSP00000382791.1:p.Ser681Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1997C>T
  hgvsp: ENSP00000373777.3:p.Ser666Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2048C>T
  hgvsp: ENSP00000446326.1:p.Ser683Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5260G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1997C>T
  hgvsp: ENSP00000382798.1:p.Ser666Phe
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser681Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

21-30949383-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949383
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949383
    reference: chr 21
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2037G>A
  hgvsp: ENST00000309434.7:c.2037G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2031G>A
  hgvsp: ENST00000399913.1:c.2031G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2031G>A
  hgvsp: ENST00000399907.1:c.2031G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20507C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1986G>A
  hgvsp: ENST00000399909.1:c.1986G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1986G>A
  hgvsp: ENST00000389125.3:c.1986G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2031G>A
  hgvsp: ENST00000389124.2:c.2031G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1986G>A
  hgvsp: ENST00000399914.1:c.1986G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2031G>A
  hgvsp: ENST00000327783.4:c.2031G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2037G>A
  hgvsp: ENST00000535441.1:c.2037G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5249C>T
  variant of: http://identifiers.org/hgnc/935
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu677Glu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

21-30949390-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949390
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949390
    reference: chr 21
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20500G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1979C>T
  hgvsp: ENSP00000373777.3:p.Thr660Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2024C>T
  hgvsp: ENSP00000382791.1:p.Thr675Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2024C>T
  hgvsp: ENSP00000382797.1:p.Thr675Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1979C>T
  hgvsp: ENSP00000382798.1:p.Thr660Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2024C>T
  hgvsp: ENSP00000373776.2:p.Thr675Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5242G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2024C>T
  hgvsp: ENSP00000327687.4:p.Thr675Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1979C>T
  hgvsp: ENSP00000382793.1:p.Thr660Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2030C>T
  hgvsp: ENSP00000311646.7:p.Thr677Ile
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2030C>T
  hgvsp: ENSP00000446326.1:p.Thr677Ile
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr675Ile
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

21-30949413-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949413
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949413
    reference: chr 21
allele count: 48
allele frequency: 3.953610964681075e-4
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1956G>A
  hgvsp: ENST00000389125.3:c.1956G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2001G>A
  hgvsp: ENST00000327783.4:c.2001G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2001G>A
  hgvsp: ENST00000399913.1:c.2001G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1956G>A
  hgvsp: ENST00000399914.1:c.1956G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2007G>A
  hgvsp: ENST00000535441.1:c.2007G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2001G>A
  hgvsp: ENST00000389124.2:c.2001G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2007G>A
  hgvsp: ENST00000309434.7:c.2007G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20477C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1956G>A
  hgvsp: ENST00000399909.1:c.1956G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2001G>A
  hgvsp: ENST00000399907.1:c.2001G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5219C>T
  variant of: http://identifiers.org/hgnc/935
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 9.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr667Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

21-30949414-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949414
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949414
    reference: chr 21
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2006C>T
  hgvsp: ENSP00000311646.7:p.Thr669Met
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1955C>T
  hgvsp: ENSP00000382793.1:p.Thr652Met
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2006C>T
  hgvsp: ENSP00000446326.1:p.Thr669Met
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.2000C>T
  hgvsp: ENSP00000382791.1:p.Thr667Met
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1955C>T
  hgvsp: ENSP00000373777.3:p.Thr652Met
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5218G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1955C>T
  hgvsp: ENSP00000382798.1:p.Thr652Met
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.2000C>T
  hgvsp: ENSP00000327687.4:p.Thr667Met
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20476G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.2000C>T
  hgvsp: ENSP00000373776.2:p.Thr667Met
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.2000C>T
  hgvsp: ENSP00000382797.1:p.Thr667Met
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr667Met
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

21-30949420-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949420
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949420
    reference: chr 21
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1994C>T
  hgvsp: ENSP00000373776.2:p.Ser665Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1994C>T
  hgvsp: ENSP00000382791.1:p.Ser665Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1949C>T
  hgvsp: ENSP00000373777.3:p.Ser650Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1949C>T
  hgvsp: ENSP00000382798.1:p.Ser650Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5212G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1994C>T
  hgvsp: ENSP00000327687.4:p.Ser665Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.2000C>T
  hgvsp: ENSP00000311646.7:p.Ser667Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1949C>T
  hgvsp: ENSP00000382793.1:p.Ser650Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20470G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.2000C>T
  hgvsp: ENSP00000446326.1:p.Ser667Phe
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1994C>T
  hgvsp: ENSP00000382797.1:p.Ser665Phe
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ser665Phe
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

21-30949456-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949456
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949456
    reference: chr 21
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1913G>A
  hgvsp: ENSP00000373777.3:p.Gly638Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1913G>A
  hgvsp: ENSP00000382793.1:p.Gly638Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1964G>A
  hgvsp: ENSP00000311646.7:p.Gly655Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1958G>A
  hgvsp: ENSP00000382791.1:p.Gly653Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5176C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1958G>A
  hgvsp: ENSP00000373776.2:p.Gly653Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1958G>A
  hgvsp: ENSP00000382797.1:p.Gly653Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1958G>A
  hgvsp: ENSP00000327687.4:p.Gly653Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1913G>A
  hgvsp: ENSP00000382798.1:p.Gly638Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1964G>A
  hgvsp: ENSP00000446326.1:p.Gly655Glu
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20434C>T
  variant of: http://identifiers.org/hgnc/935
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly653Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

21-30949473-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949473
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949473
    reference: chr 21
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1941G>A
  hgvsp: ENST00000389124.2:c.1941G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1896G>A
  hgvsp: ENST00000389125.3:c.1896G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1941G>A
  hgvsp: ENST00000399913.1:c.1941G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1941G>A
  hgvsp: ENST00000327783.4:c.1941G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20417C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5159C>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1896G>A
  hgvsp: ENST00000399914.1:c.1896G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1896G>A
  hgvsp: ENST00000399909.1:c.1896G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1947G>A
  hgvsp: ENST00000535441.1:c.1947G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1947G>A
  hgvsp: ENST00000309434.7:c.1947G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1941G>A
  hgvsp: ENST00000399907.1:c.1941G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser647Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS

21-30949489-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949489
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949489
    reference: chr 21
allele count: 1
allele frequency: 8.269383434771103e-6
allele num: 120928
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1925T>C
  hgvsp: ENSP00000382791.1:p.Met642Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5143A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1931T>C
  hgvsp: ENSP00000446326.1:p.Met644Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1880T>C
  hgvsp: ENSP00000382798.1:p.Met627Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1925T>C
  hgvsp: ENSP00000382797.1:p.Met642Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1880T>C
  hgvsp: ENSP00000382793.1:p.Met627Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1931T>C
  hgvsp: ENSP00000311646.7:p.Met644Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1880T>C
  hgvsp: ENSP00000373777.3:p.Met627Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1925T>C
  hgvsp: ENSP00000327687.4:p.Met642Thr
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20401A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1925T>C
  hgvsp: ENSP00000373776.2:p.Met642Thr
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met642Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

21-30949507-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949507
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949507
    reference: chr 21
allele count: 2
allele frequency: 1.661074382910867e-5
allele num: 120404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5125A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1913-6T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1913-6T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1913-6T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1919-6T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20383A>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1913-6T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1868-6T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1868-6T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1919-6T>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1868-6T>C
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1913-6T>C
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

21-30949507-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949507
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949507
    reference: chr 21
allele count: 2
allele frequency: 1.661074382910867e-5
allele num: 120404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1868-6T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5125A>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1913-6T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1913-6T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1913-6T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1913-6T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1919-6T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1868-6T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1919-6T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20383A>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1868-6T>A
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1913-6T>A
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

21-30949521-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949521
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949521
    reference: chr 21
allele count: 1
allele frequency: 8.344598541364175e-6
allele num: 119838
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1913-20C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1913-20C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20369G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1913-20C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1868-20C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1919-20C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5111G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1868-20C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1868-20C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1913-20C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1919-20C>T
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

21-30949526-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949526
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949526
    reference: chr 21
allele count: 1
allele frequency: 8.354498061756449e-6
allele num: 119696
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1913-25C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1868-25C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1868-25C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1913-25C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20364G>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1868-25C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1913-25C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5106G>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1913-25C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1919-25C>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1919-25C>G
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

21-30949526-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949526
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949526
    reference: chr 21
allele count: 1
allele frequency: 8.354498061756449e-6
allele num: 119696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1919-25C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1868-25C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5106G>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1913-25C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20364G>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1913-25C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1868-25C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1913-25C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1868-25C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1913-25C>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1919-25C>A
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

21-30949527-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949527
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949527
    reference: chr 21
allele count: 4
allele frequency: 3.343251646551436e-5
allele num: 119644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20363G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1913-26C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1919-26C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1868-26C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1868-26C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1919-26C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5105G>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1913-26C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1913-26C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1913-26C>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1868-26C>T
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8373
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS

21-30949533-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949533
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949533
    reference: chr 21
allele count: 2
allele frequency: 1.675069934169752e-5
allele num: 119398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1868-32T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1868-32T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20357A>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1913-32T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1868-32T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1913-32T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1919-32T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1913-32T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5099A>T
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1913-32T>A
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1919-32T>A
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/21-30949535-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949535
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949535
    reference: chr 21
allele count: 1
allele frequency: 8.388558006878617e-6
allele num: 119210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1919-34G>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5097C>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1868-34G>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1913-34G>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1913-34G>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1913-34G>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1919-34G>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1868-34G>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1868-34G>T
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20355C>A
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1913-34G>T
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

21-30949535-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949535
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949535
    reference: chr 21
allele count: 1
allele frequency: 8.388558006878617e-6
allele num: 119210
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1913-34G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1913-34G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1913-34G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1868-34G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20355C>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5097C>G
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1919-34G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1868-34G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1913-34G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1868-34G>C
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1919-34G>C
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

21-30949536-ACAGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949536
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949532
    reference: chr 21
allele count: 1
allele frequency: 8.387432271484408e-6
allele num: 119226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1868-39_1868-36delACTG
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1868-39_1868-36delACTG
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1913-39_1913-36delACTG
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1868-39_1868-36delACTG
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1913-39_1913-36delACTG
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5092_473-5089delTCAG
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1919-39_1919-36delACTG
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20350_326-20347delTCAG
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1913-39_1913-36delACTG
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1919-39_1919-36delACTG
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1913-39_1913-36delACTG
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: ACAGT
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/21-30949538-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30949538
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 30949538
    reference: chr 21
allele count: 1
allele frequency: 8.402937667008386e-6
allele num: 119006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382793
  ensembl transcript: ENST00000399909
  gene symbol: GRIK1
  hgvsc: ENST00000399909.1:c.1868-37T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000311646
  ensembl transcript: ENST00000309434
  gene symbol: GRIK1
  hgvsc: ENST00000309434.7:c.1919-37T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000416569
  ensembl transcript: ENST00000422809
  gene symbol: BACH1
  hgvsc: ENST00000422809.1:c.473-5094A>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382797
  ensembl transcript: ENST00000399913
  gene symbol: GRIK1
  hgvsc: ENST00000399913.1:c.1913-37T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000156273
  ensembl protein: ENSP00000470673
  ensembl transcript: ENST00000468059
  gene symbol: BACH1
  hgvsc: ENST00000468059.1:c.326-20352A>C
  variant of: http://identifiers.org/hgnc/935
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000446326
  ensembl transcript: ENST00000535441
  gene symbol: GRIK1
  hgvsc: ENST00000535441.1:c.1919-37T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373776
  ensembl transcript: ENST00000389124
  gene symbol: GRIK1
  hgvsc: ENST00000389124.2:c.1913-37T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000373777
  ensembl transcript: ENST00000389125
  gene symbol: GRIK1
  hgvsc: ENST00000389125.3:c.1868-37T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382798
  ensembl transcript: ENST00000399914
  gene symbol: GRIK1
  hgvsc: ENST00000399914.1:c.1868-37T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000382791
  ensembl transcript: ENST00000399907
  gene symbol: GRIK1
  hgvsc: ENST00000399907.1:c.1913-37T>G
  variant of: http://identifiers.org/hgnc/4579
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171189
  ensembl protein: ENSP00000327687
  ensembl transcript: ENST00000327783
  gene symbol: GRIK1
  hgvsc: ENST00000327783.4:c.1913-37T>G
  variant of: http://identifiers.org/hgnc/4579
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6684
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8816
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 114
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49459
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 992
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2385
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 5301
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.508e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.69e-1

QD
type: SiteQuality
SIO_000300: 1.156e1

FS
type: SiteQuality
SIO_000300: 1.0695e1

DP
type: SiteQuality
SIO_000300: 1.592975e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 5.927e1

GenotypeDepth
all individuals: 243
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49365
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 306
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5299
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1074
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 507
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: -8.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e0

FS
type: SiteQuality
SIO_000300: 9.79e-1

DP
type: SiteQuality
SIO_000300: 1.592239e6

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 1.533e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 114
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2401
bin: 9.75e1
variant carriers: 20

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

GenotypeQuality
all individuals: 980
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 214
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49176
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 2.25e1
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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Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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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: 1.158960595339759e-3
allele num: 16394
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

FS
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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SIO_000300: 9.8e-1

VQSLOD
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DP
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SIO_000300: 1.591525e6

QD
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SIO_000300: 1.174e1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

Other
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele num: 10366
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South Asian
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East Asian
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allele frequency: 1.157943492357573e-4
allele num: 8636
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Latino
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FS
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InbreedingCoeff
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QD
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BaseQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10340
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8632
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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South Asian
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Latino
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allele frequency: 8.756567425569177e-5
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European (Non-Finnish)
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allele frequency: 0.0e0
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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QD
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11396
num of homozygotes: 0

Other
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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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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507022725902707e-5
allele num: 66356
num of homozygotes: 0

East Asian
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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

African
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ReadPosRankSum
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SIO_000300: 8.52e-1

BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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ClippingRankSum
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VQSLOD
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QD
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11262
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65846
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ClippingRankSum
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FS
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BaseQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11094
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

East Asian
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Other
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South Asian
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African
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European (Non-Finnish)
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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MQ
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QD
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 64172
num of homozygotes: 0

East Asian
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European (Finnish)
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Other
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South Asian
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Latino
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African
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6078
num of homozygotes: 0

Latino
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African
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Other
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East Asian
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European (Non-Finnish)
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South Asian
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MQ
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ReadPosRankSum
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MQRankSum
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FS
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Finnish)
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East Asian
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Other
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European (Non-Finnish)
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African
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DP
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FS
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MQ
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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Other
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 15018
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East Asian
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African
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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Latino
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Other
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South Asian
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European (Finnish)
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QD
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FS
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

European (Non-Finnish)
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South Asian
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European (Finnish)
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African
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Other
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East Asian
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QD
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ReadPosRankSum
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BaseQRankSum
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FS
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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QD
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ReadPosRankSum
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FS
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DP
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MQ
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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South Asian
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BaseQRankSum
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DP
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
SIO_000300: 2.296e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 12157
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variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46356
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.271617497456765e-4
allele num: 7864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.524e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.276e0

DP
type: SiteQuality
SIO_000300: 1.007887e6

VQSLOD
type: SiteQuality
SIO_000300: -8.335e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

QD
type: SiteQuality
SIO_000300: 1.147e1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.69092083310909e-5
allele num: 37162
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11712
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.58924e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.098e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

QD
type: SiteQuality
SIO_000300: 8.08e0

VQSLOD
type: SiteQuality
SIO_000300: -1.308e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 286
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GenotypeQuality
all individuals: 5573
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4936
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35068
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3318
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.753501400560224e-5
allele num: 11424
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-2

DP
type: SiteQuality
SIO_000300: 8.37289e5

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

QD
type: SiteQuality
SIO_000300: 9.35e0

MQ
type: SiteQuality
SIO_000300: 5.662e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e0

FS
type: SiteQuality
SIO_000300: 3.274e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.359e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2371
bin: 9.75e1
variant carriers: 11

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5428
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 6.157635467980296e-4
allele num: 3248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2484
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 7.835455435847208e-4
allele num: 10210
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.192982456140351e-3
allele num: 456
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.76097e5

MQRankSum
type: SiteQuality
SIO_000300: -6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.32e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
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SIO_000300: -1.159e0

DP
type: SiteQuality
SIO_000300: 7.75063e5

FS
type: SiteQuality
SIO_000300: 0.0e0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.522533495736906e-5
allele num: 65680
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14976
num of homozygotes: 0

African
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: 874
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65844
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.979414093428345e-4
allele num: 15156
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.58e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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DP
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SIO_000300: 2.099927e6

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

South Asian
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Other
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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
allele num: 8550
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.514233797698365e-5
allele num: 66040
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: 1.9e-3

VQSLOD
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QD
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BaseQRankSum
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FS
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DP
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SIO_000300: 2.113321e6

MQ
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: -1.868e0

MQRankSum
type: SiteQuality
SIO_000300: -1.502e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 5.217391304347826e-4
allele num: 11500
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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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ClippingRankSum
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DP
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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FS
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QD
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MQ
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SIO_000300: 5.963e1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.514325519413653e-5
allele num: 66036
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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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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European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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FS
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QD
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DP
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SIO_000300: 2.11495e6

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

South Asian
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allele count: 1
allele frequency: 6.436663233779608e-5
allele num: 15536
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66102
num of homozygotes: 0

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

European (Finnish)
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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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Other
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East Asian
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DP
type: SiteQuality
SIO_000300: 2.11795e6

FS
type: SiteQuality
SIO_000300: 1.985e0

MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
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QD
type: SiteQuality
SIO_000300: 1.737e1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66114
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 888
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Latino
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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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African
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allele num: 10302
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East Asian
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European (Finnish)
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QD
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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Latino
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South Asian
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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Latino
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Other
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South Asian
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European (Finnish)
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MQ
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ReadPosRankSum
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MQRankSum
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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South Asian
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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allele frequency: 4.507482420818559e-5
allele num: 66556
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
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BaseQRankSum
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QD
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

Other
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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: 6612
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -3.81e0

MQ
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SIO_000300: 5.984e1

ReadPosRankSum
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SIO_000300: -3.82e-1

FS
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VQSLOD
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DP
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: 9.79e-1

InbreedingCoeff
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SIO_000300: 3.9e-2

GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

Other
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South Asian
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allele num: 16382
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East Asian
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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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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -6.46e-1

DP
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BaseQRankSum
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ReadPosRankSum
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QD
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SIO_000300: 6.89e0

MQRankSum
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SIO_000300: 1.4e-2

InbreedingCoeff
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SIO_000300: 3.86e-2

FS
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.268e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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variant carriers: 0

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

Latino
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East Asian
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European (Finnish)
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num of homozygotes: 0

Other
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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MQRankSum
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DP
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MQ
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ReadPosRankSum
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SIO_000300: -7.84e-1

GenotypeDepth
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variant carriers: 0

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

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

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

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

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 66640
num of homozygotes: 0

European (Finnish)
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VQSLOD
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ClippingRankSum
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QD
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ReadPosRankSum
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MQRankSum
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DP
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BaseQRankSum
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MQ
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SIO_000300: 5.93e1

FS
type: SiteQuality
SIO_000300: 1.1276e1

InbreedingCoeff
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SIO_000300: 4.29e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

South Asian
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allele num: 16484
num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

BaseQRankSum
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SIO_000300: 1.31e0

MQRankSum
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QD
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 12

African
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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

European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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Other
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Latino
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East Asian
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BaseQRankSum
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InbreedingCoeff
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QD
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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DP
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele count: 2
allele frequency: 1.21256214380987e-4
allele num: 16494
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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East Asian
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African
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Other
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BaseQRankSum
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MQRankSum
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MQ
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QD
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ClippingRankSum
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FS
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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Latino
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Other
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African
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South Asian
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InbreedingCoeff
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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MQRankSum
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FS
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ReadPosRankSum
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DP
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SIO_000300: 2.151336e6

GenotypeDepth
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variant carriers: 0

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

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

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

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66712
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African
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Other
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South Asian
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East Asian
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MQ
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MQRankSum
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

Other
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
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FS
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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East Asian
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South Asian
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ReadPosRankSum
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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DP
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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ReadPosRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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FS
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ClippingRankSum
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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African
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allele num: 10404
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Latino
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allele frequency: 0.0e0
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South Asian
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BaseQRankSum
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QD
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FS
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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InbreedingCoeff
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Latino
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South Asian
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Other
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East Asian
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QD
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VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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East Asian
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Other
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Latino
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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QD
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Non-Finnish)
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South Asian
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Other
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European (Finnish)
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BaseQRankSum
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

South Asian
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allele num: 16510
num of homozygotes: 0

Other
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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QD
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MQ
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InbreedingCoeff
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DP
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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African
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Other
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MQ
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MQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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South Asian
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Other
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European (Non-Finnish)
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Latino
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.152446e6

FS
type: SiteQuality
SIO_000300: 1.024e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.022e0

InbreedingCoeff
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SIO_000300: 5.1e-3

BaseQRankSum
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SIO_000300: -4.258e0

QD
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SIO_000300: 9.41e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: -6.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.3e-3

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
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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: 8654
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

QD
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SIO_000300: 1.075e1

FS
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 1.0e-4

ReadPosRankSum
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BaseQRankSum
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SIO_000300: -3.387e0

MQRankSum
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SIO_000300: 6.1e-2

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 2.151493e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

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

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

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

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

South Asian
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allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-1

BaseQRankSum
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SIO_000300: 5.33e0

InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
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DP
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SIO_000300: 2.149429e6

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.16e-1

FS
type: SiteQuality
SIO_000300: 3.968e0

GenotypeDepth
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variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 61
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

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

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

East 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
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
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SIO_000300: -1.492e0

MQ
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.159e1

VQSLOD
type: SiteQuality
SIO_000300: 2.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeDepth
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505253334136135e-5
allele num: 66434
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 898
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 5.17e-1

MQ
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DP
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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SIO_000300: 1.92e0

ClippingRankSum
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SIO_000300: -8.599999999999999e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.01050666827227e-5
allele num: 66434
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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DP
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MQ
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 2.71e0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50879628232596e-5
allele num: 66278
num of homozygotes: 0

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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Other
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VQSLOD
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MQ
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10270
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509798592867711e-5
allele num: 66234
num of homozygotes: 0

South Asian
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European (Finnish)
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num of homozygotes: 0

Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
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ReadPosRankSum
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DP
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MQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509798592867711e-5
allele num: 66234
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.048e0

DP
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.74e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 9.7e-1

MQRankSum
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SIO_000300: -1.962e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510072181450273e-5
allele num: 66222
num of homozygotes: 0

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

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

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

South Asian
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allele count: 2
allele frequency: 1.294498381877023e-4
allele num: 15450
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

MQRankSum
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SIO_000300: 2.43e-1

MQ
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SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 2.095742e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

BaseQRankSum
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SIO_000300: -2.212e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.64e-1

QD
type: SiteQuality
SIO_000300: 1.401e1

FS
type: SiteQuality
SIO_000300: 1.997e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 15288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66184
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

Latino
type: Population
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allele frequency: 1.730403183941858e-4
allele num: 11558
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.37e-1

ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: -3.14e0

QD
type: SiteQuality
SIO_000300: 1.333e1

MQRankSum
type: SiteQuality
SIO_000300: -1.53e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
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: 884
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.512172992590352e-5
allele num: 66130
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15168
num of homozygotes: 0

African
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allele count: 0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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SIO_000300: 1.248e1

MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15168
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.512172992590352e-5
allele num: 66130
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10216
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66130
num of homozygotes: 0

East Asian
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allele count: 0
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num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.583278472679394e-5
allele num: 15190
num of homozygotes: 0

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

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

Other
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

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