http://identifiers.org/exac.variant/18-3567514-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567514
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567514
    reference: chr 18
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.2031G>T
  hgvsp: ENST00000515196.2:c.2031G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1101G>T
  hgvsp: ENST00000400149.3:c.1101G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1149G>T
  hgvsp: ENST00000400155.1:c.1149G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1155G>T
  hgvsp: ENST00000539435.1:c.1155G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1179G>T
  hgvsp: ENST00000400150.3:c.1179G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.2031G>T
  hgvsp: ENST00000315677.3:c.2031G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1083G>T
  hgvsp: ENST00000534970.1:c.1083G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1149G>T
  hgvsp: ENST00000581699.1:c.1149G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1125G>T
  hgvsp: ENST00000400145.2:c.1125G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1125G>T
  hgvsp: ENST00000400147.2:c.1125G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.2031G>T
  hgvsp: ENST00000584874.1:c.2031G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.2031G>T
  hgvsp: ENST00000581527.1:c.2031G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val677Val
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

18-3567516-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567516
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567516
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1177G>A
  hgvsp: ENSP00000383014.3:p.Val393Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1123G>A
  hgvsp: ENSP00000383011.2:p.Val375Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.2029G>A
  hgvsp: ENSP00000462882.1:p.Val677Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1099G>A
  hgvsp: ENSP00000383013.3:p.Val367Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.2029G>A
  hgvsp: ENSP00000316377.3:p.Val677Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1147G>A
  hgvsp: ENSP00000462848.1:p.Val383Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1147G>A
  hgvsp: ENSP00000383019.1:p.Val383Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.2029G>A
  hgvsp: ENSP00000463864.1:p.Val677Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.2029G>A
  hgvsp: ENSP00000445973.1:p.Val677Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1123G>A
  hgvsp: ENSP00000383010.2:p.Val375Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1153G>A
  hgvsp: ENSP00000446312.1:p.Val385Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1081G>A
  hgvsp: ENSP00000437817.1:p.Val361Met
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
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: 1707
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val677Met
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

18-3567517-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567517
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567517
    reference: chr 18
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1080C>T
  hgvsp: ENST00000534970.1:c.1080C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1098C>T
  hgvsp: ENST00000400149.3:c.1098C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1152C>T
  hgvsp: ENST00000539435.1:c.1152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1176C>T
  hgvsp: ENST00000400150.3:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.2028C>T
  hgvsp: ENST00000584874.1:c.2028C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.2028C>T
  hgvsp: ENST00000315677.3:c.2028C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.2028C>T
  hgvsp: ENST00000515196.2:c.2028C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1146C>T
  hgvsp: ENST00000581699.1:c.1146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1122C>T
  hgvsp: ENST00000400145.2:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.2028C>T
  hgvsp: ENST00000581527.1:c.2028C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1122C>T
  hgvsp: ENST00000400147.2:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1146C>T
  hgvsp: ENST00000400155.1:c.1146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser676Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

18-3567535-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567535
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567535
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.2010A>G
  hgvsp: ENST00000315677.3:c.2010A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1080A>G
  hgvsp: ENST00000400149.3:c.1080A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1104A>G
  hgvsp: ENST00000400145.2:c.1104A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.2010A>G
  hgvsp: ENST00000584874.1:c.2010A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1134A>G
  hgvsp: ENST00000539435.1:c.1134A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1062A>G
  hgvsp: ENST00000534970.1:c.1062A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1158A>G
  hgvsp: ENST00000400150.3:c.1158A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1128A>G
  hgvsp: ENST00000581699.1:c.1128A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1128A>G
  hgvsp: ENST00000400155.1:c.1128A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1104A>G
  hgvsp: ENST00000400147.2:c.1104A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.2010A>G
  hgvsp: ENST00000581527.1:c.2010A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.2010A>G
  hgvsp: ENST00000515196.2:c.2010A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala670Ala
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

18-3567546-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567546
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567546
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1117G>C
  hgvsp: ENSP00000462848.1:p.Glu373Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1999G>C
  hgvsp: ENSP00000316377.3:p.Glu667Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1069G>C
  hgvsp: ENSP00000383013.3:p.Glu357Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1117G>C
  hgvsp: ENSP00000383019.1:p.Glu373Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1999G>C
  hgvsp: ENSP00000445973.1:p.Glu667Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1147G>C
  hgvsp: ENSP00000383014.3:p.Glu383Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1123G>C
  hgvsp: ENSP00000446312.1:p.Glu375Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1093G>C
  hgvsp: ENSP00000383010.2:p.Glu365Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1999G>C
  hgvsp: ENSP00000462882.1:p.Glu667Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1093G>C
  hgvsp: ENSP00000383011.2:p.Glu365Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1999G>C
  hgvsp: ENSP00000463864.1:p.Glu667Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1051G>C
  hgvsp: ENSP00000437817.1:p.Glu351Gln
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu667Gln
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

18-3567556-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567556
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567556
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1989C>A
  hgvsp: ENSP00000462882.1:p.Asp663Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1137C>A
  hgvsp: ENSP00000383014.3:p.Asp379Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1041C>A
  hgvsp: ENSP00000437817.1:p.Asp347Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1989C>A
  hgvsp: ENSP00000316377.3:p.Asp663Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1989C>A
  hgvsp: ENSP00000445973.1:p.Asp663Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1113C>A
  hgvsp: ENSP00000446312.1:p.Asp371Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1989C>A
  hgvsp: ENSP00000463864.1:p.Asp663Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1059C>A
  hgvsp: ENSP00000383013.3:p.Asp353Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1107C>A
  hgvsp: ENSP00000462848.1:p.Asp369Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1083C>A
  hgvsp: ENSP00000383010.2:p.Asp361Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1107C>A
  hgvsp: ENSP00000383019.1:p.Asp369Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1083C>A
  hgvsp: ENSP00000383011.2:p.Asp361Glu
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp663Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

18-3567568-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567568
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567568
    reference: chr 18
allele count: 430
allele frequency: 3.54206823835648e-3
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1125T>C
  hgvsp: ENST00000400150.3:c.1125T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1977T>C
  hgvsp: ENST00000515196.2:c.1977T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1047T>C
  hgvsp: ENST00000400149.3:c.1047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1977T>C
  hgvsp: ENST00000581527.1:c.1977T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1095T>C
  hgvsp: ENST00000581699.1:c.1095T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1071T>C
  hgvsp: ENST00000400145.2:c.1071T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1977T>C
  hgvsp: ENST00000584874.1:c.1977T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1977T>C
  hgvsp: ENST00000315677.3:c.1977T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1071T>C
  hgvsp: ENST00000400147.2:c.1071T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1095T>C
  hgvsp: ENST00000400155.1:c.1095T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1029T>C
  hgvsp: ENST00000534970.1:c.1029T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1101T>C
  hgvsp: ENST00000539435.1:c.1101T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 9.75e1
  variant carriers: 332
genotype depth: GenotypeDepth
  all individuals: 7856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6320
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
hgvs: p.Ala659Ala
num of homozygotes: 4
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

18-3567595-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567595
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567595
    reference: chr 18
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1966-16T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1084-16T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1036-16T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1060-16T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1060-16T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1018-16T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1966-16T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1090-16T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1966-16T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1114-16T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1084-16T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1966-16T>C
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

18-3567604-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567604
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567604
    reference: chr 18
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1966-25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1084-25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1036-25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1060-25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1114-25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1060-25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1966-25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1084-25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1966-25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1090-25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1018-25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1966-25T>C
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

18-3567605-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567605
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567605
    reference: chr 18
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1060-26C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1018-26C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1966-26C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1966-26C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1114-26C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1966-26C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1084-26C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1090-26C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1966-26C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1084-26C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1060-26C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1036-26C>T
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7857
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

18-3567612-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567612
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567612
    reference: chr 18
allele count: 2
allele frequency: 1.648614339647526e-5
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1966-33G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1060-33G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1084-33G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1060-33G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1090-33G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1036-33G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1018-33G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1966-33G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1966-33G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1084-33G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1966-33G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1114-33G>A
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-3567613-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567613
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567613
    reference: chr 18
allele count: 3
allele frequency: 2.472799208704253e-5
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1966-34T>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1084-34T>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1060-34T>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1966-34T>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1084-34T>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1060-34T>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1966-34T>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1036-34T>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1966-34T>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1018-34T>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1090-34T>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1114-34T>G
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

18-3567618-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567618
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567618
    reference: chr 18
allele count: 4
allele frequency: 3.297717979158422e-5
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1060-39T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1084-39T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1114-39T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1966-39T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1966-39T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1036-39T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1084-39T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1060-39T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1966-39T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1090-39T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1966-39T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1018-39T>C
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

18-3567623-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567623
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567623
    reference: chr 18
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1084-44A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1084-44A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1966-44A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1966-44A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1036-44A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1114-44A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1966-44A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1060-44A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1060-44A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1018-44A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1090-44A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1966-44A>G
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

18-3567631-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567631
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567631
    reference: chr 18
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1018-52C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1084-52C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1966-52C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1060-52C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1090-52C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1966-52C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1084-52C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1114-52C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1060-52C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1036-52C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1966-52C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1966-52C>G
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7833
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

18-3567631-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3567631
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3567630
    reference: chr 18
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1966-53delT
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1060-53delT
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1090-53delT
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1966-53delT
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1084-53delT
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1114-53delT
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1018-53delT
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1060-53delT
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1036-53delT
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1966-53delT
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1966-53delT
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1084-53delT
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: GA
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD

18-3581823-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581823
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581823
    reference: chr 18
allele count: 1
allele frequency: 8.397997917296517e-6
allele num: 119076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1059+50A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1089+50A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1083+50A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1017+50A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1113+50A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1965+50A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1035+50A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1083+50A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1965+50A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1059+50A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1965+50A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1965+50A>G
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

18-3581829-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581829
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581829
    reference: chr 18
allele count: 1
allele frequency: 8.393768466290626e-6
allele num: 119136
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1965+44T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1965+44T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1965+44T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1083+44T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1035+44T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1059+44T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1113+44T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1089+44T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1059+44T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1083+44T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1017+44T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1965+44T>C
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

18-3581832-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581832
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581832
    reference: chr 18
allele count: 1
allele frequency: 8.389824820457749e-6
allele num: 119192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1965+41A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1965+41A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1089+41A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1059+41A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1059+41A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1083+41A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1017+41A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1035+41A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1083+41A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1965+41A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1965+41A>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1113+41A>G
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

18-3581838-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581838
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581838
    reference: chr 18
allele count: 2
allele frequency: 1.676333523317799e-5
allele num: 119308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1035+35A>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1965+35A>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1059+35A>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1059+35A>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1083+35A>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1965+35A>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1083+35A>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1113+35A>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1965+35A>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1017+35A>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1965+35A>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1089+35A>T
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

18-3581841-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581841
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581841
    reference: chr 18
allele count: 1
allele frequency: 8.373245805003851e-6
allele num: 119428
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1089+32G>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1965+32G>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1035+32G>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1059+32G>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1965+32G>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1083+32G>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1017+32G>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1965+32G>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1113+32G>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1965+32G>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1059+32G>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1083+32G>C
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

18-3581848-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581848
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581848
    reference: chr 18
allele count: 2
allele frequency: 1.66858554003771e-5
allele num: 119862
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1089+25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1017+25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1965+25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1059+25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1035+25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1059+25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1083+25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1965+25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1083+25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1965+25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1113+25T>C
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1965+25T>C
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD

18-3581853-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581853
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581854
    reference: chr 18
allele count: 5
allele frequency: 4.158695832986775e-5
allele num: 120230
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1059+19dupA
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1965+19dupA
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1017+19dupA
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1059+19dupA
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1965+19dupA
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1965+19dupA
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1965+19dupA
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1035+19dupA
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1083+19dupA
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1083+19dupA
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1113+19dupA
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1089+19dupA
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

18-3581860-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581860
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581860
    reference: chr 18
allele count: 8
allele frequency: 6.625368536124821e-5
allele num: 120748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1965+13C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1965+13C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1083+13C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1083+13C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1059+13C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1089+13C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1017+13C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1965+13C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1965+13C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1113+13C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1035+13C>G
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1059+13C>G
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3061
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

18-3581862-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581862
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581862
    reference: chr 18
allele count: 1
allele frequency: 8.271982794275789e-6
allele num: 120890
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1059+11C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1965+11C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1089+11C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1017+11C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1035+11C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1059+11C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1083+11C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1113+11C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1965+11C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1965+11C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1083+11C>T
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1965+11C>T
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

18-3581866-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581866
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581866
    reference: chr 18
allele count: 1
allele frequency: 8.263779852904718e-6
allele num: 121010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1083+7G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1965+7G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1083+7G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1965+7G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1089+7G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1035+7G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1017+7G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1059+7G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1113+7G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1965+7G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1059+7G>A
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1965+7G>A
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1965+7G>A
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

18-3581878-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581878
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581878
    reference: chr 18
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1054A>G
  hgvsp: ENSP00000383011.2:p.Ile352Val
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1012A>G
  hgvsp: ENSP00000437817.1:p.Ile338Val
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1030A>G
  hgvsp: ENSP00000383013.3:p.Ile344Val
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1960A>G
  hgvsp: ENSP00000316377.3:p.Ile654Val
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1054A>G
  hgvsp: ENSP00000383010.2:p.Ile352Val
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1960A>G
  hgvsp: ENSP00000462882.1:p.Ile654Val
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1078A>G
  hgvsp: ENSP00000383019.1:p.Ile360Val
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1108A>G
  hgvsp: ENSP00000383014.3:p.Ile370Val
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1084A>G
  hgvsp: ENSP00000446312.1:p.Ile362Val
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1078A>G
  hgvsp: ENSP00000462848.1:p.Ile360Val
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1960A>G
  hgvsp: ENSP00000463864.1:p.Ile654Val
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1960A>G
  hgvsp: ENSP00000445973.1:p.Ile654Val
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile654Val
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

18-3581879-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581879
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581879
    reference: chr 18
allele count: 21
allele frequency: 1.731501789218515e-4
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1959G>A
  hgvsp: ENST00000315677.3:c.1959G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1053G>A
  hgvsp: ENST00000400147.2:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1011G>A
  hgvsp: ENST00000534970.1:c.1011G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1077G>A
  hgvsp: ENST00000581699.1:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1029G>A
  hgvsp: ENST00000400149.3:c.1029G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1053G>A
  hgvsp: ENST00000400145.2:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1959G>A
  hgvsp: ENST00000581527.1:c.1959G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1077G>A
  hgvsp: ENST00000400155.1:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1107G>A
  hgvsp: ENST00000400150.3:c.1107G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1083G>A
  hgvsp: ENST00000539435.1:c.1083G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1959G>A
  hgvsp: ENST00000584874.1:c.1959G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1959G>A
  hgvsp: ENST00000515196.2:c.1959G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly653Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

18-3581882-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581882
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581882
    reference: chr 18
allele count: 3
allele frequency: 2.472921509471289e-5
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1956C>T
  hgvsp: ENST00000315677.3:c.1956C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1074C>T
  hgvsp: ENST00000400155.1:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1956C>T
  hgvsp: ENST00000515196.2:c.1956C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1080C>T
  hgvsp: ENST00000539435.1:c.1080C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1956C>T
  hgvsp: ENST00000584874.1:c.1956C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1104C>T
  hgvsp: ENST00000400150.3:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1026C>T
  hgvsp: ENST00000400149.3:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1050C>T
  hgvsp: ENST00000400147.2:c.1050C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1956C>T
  hgvsp: ENST00000581527.1:c.1956C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1074C>T
  hgvsp: ENST00000581699.1:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1050C>T
  hgvsp: ENST00000400145.2:c.1050C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1008C>T
  hgvsp: ENST00000534970.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5010
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile652Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

18-3581888-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581888
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581888
    reference: chr 18
allele count: 3
allele frequency: 2.472024918011174e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1020G>A
  hgvsp: ENST00000400149.3:c.1020G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1950G>A
  hgvsp: ENST00000584874.1:c.1950G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1098G>A
  hgvsp: ENST00000400150.3:c.1098G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1068G>A
  hgvsp: ENST00000581699.1:c.1068G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1068G>A
  hgvsp: ENST00000400155.1:c.1068G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1044G>A
  hgvsp: ENST00000400145.2:c.1044G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1044G>A
  hgvsp: ENST00000400147.2:c.1044G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.1002G>A
  hgvsp: ENST00000534970.1:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1950G>A
  hgvsp: ENST00000315677.3:c.1950G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1950G>A
  hgvsp: ENST00000581527.1:c.1950G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1950G>A
  hgvsp: ENST00000515196.2:c.1950G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1074G>A
  hgvsp: ENST00000539435.1:c.1074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5008
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu650Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

18-3581894-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581894
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581894
    reference: chr 18
allele count: 2
allele frequency: 1.647690761397901e-5
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1092A>G
  hgvsp: ENST00000400150.3:c.1092A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1014A>G
  hgvsp: ENST00000400149.3:c.1014A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1944A>G
  hgvsp: ENST00000581527.1:c.1944A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1062A>G
  hgvsp: ENST00000400155.1:c.1062A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1038A>G
  hgvsp: ENST00000400145.2:c.1038A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1944A>G
  hgvsp: ENST00000584874.1:c.1944A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1944A>G
  hgvsp: ENST00000315677.3:c.1944A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1062A>G
  hgvsp: ENST00000581699.1:c.1062A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1068A>G
  hgvsp: ENST00000539435.1:c.1068A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1038A>G
  hgvsp: ENST00000400147.2:c.1038A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1944A>G
  hgvsp: ENST00000515196.2:c.1944A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.996A>G
  hgvsp: ENST00000534970.1:c.996A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5010
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg648Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-3581894-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581894
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581894
    reference: chr 18
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1038A>T
  hgvsp: ENST00000400147.2:c.1038A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1944A>T
  hgvsp: ENST00000584874.1:c.1944A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1062A>T
  hgvsp: ENST00000581699.1:c.1062A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1068A>T
  hgvsp: ENST00000539435.1:c.1068A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1014A>T
  hgvsp: ENST00000400149.3:c.1014A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1092A>T
  hgvsp: ENST00000400150.3:c.1092A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1944A>T
  hgvsp: ENST00000315677.3:c.1944A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1038A>T
  hgvsp: ENST00000400145.2:c.1038A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.996A>T
  hgvsp: ENST00000534970.1:c.996A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1062A>T
  hgvsp: ENST00000400155.1:c.1062A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1944A>T
  hgvsp: ENST00000581527.1:c.1944A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1944A>T
  hgvsp: ENST00000515196.2:c.1944A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5010
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg648Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

18-3581895-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581895
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581895
    reference: chr 18
allele count: 53
allele frequency: 4.366308574441442e-4
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1037G>A
  hgvsp: ENSP00000383010.2:p.Arg346Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1943G>A
  hgvsp: ENSP00000445973.1:p.Arg648Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1091G>A
  hgvsp: ENSP00000383014.3:p.Arg364Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1943G>A
  hgvsp: ENSP00000462882.1:p.Arg648Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1067G>A
  hgvsp: ENSP00000446312.1:p.Arg356Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1943G>A
  hgvsp: ENSP00000316377.3:p.Arg648Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1061G>A
  hgvsp: ENSP00000383019.1:p.Arg354Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1061G>A
  hgvsp: ENSP00000462848.1:p.Arg354Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.995G>A
  hgvsp: ENSP00000437817.1:p.Arg332Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1037G>A
  hgvsp: ENSP00000383011.2:p.Arg346Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1943G>A
  hgvsp: ENSP00000463864.1:p.Arg648Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1013G>A
  hgvsp: ENSP00000383013.3:p.Arg338Gln
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5061
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Arg648Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-3581906-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581906
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581906
    reference: chr 18
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.984T>C
  hgvsp: ENST00000534970.1:c.984T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1026T>C
  hgvsp: ENST00000400145.2:c.1026T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1002T>C
  hgvsp: ENST00000400149.3:c.1002T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1932T>C
  hgvsp: ENST00000581527.1:c.1932T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1080T>C
  hgvsp: ENST00000400150.3:c.1080T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1050T>C
  hgvsp: ENST00000581699.1:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1026T>C
  hgvsp: ENST00000400147.2:c.1026T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1932T>C
  hgvsp: ENST00000315677.3:c.1932T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1932T>C
  hgvsp: ENST00000515196.2:c.1932T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1932T>C
  hgvsp: ENST00000584874.1:c.1932T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1056T>C
  hgvsp: ENST00000539435.1:c.1056T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1050T>C
  hgvsp: ENST00000400155.1:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5003
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe644Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

18-3581908-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581908
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581908
    reference: chr 18
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1930T>C
  hgvsp: ENSP00000445973.1:p.Phe644Leu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.1000T>C
  hgvsp: ENSP00000383013.3:p.Phe334Leu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1930T>C
  hgvsp: ENSP00000462882.1:p.Phe644Leu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1024T>C
  hgvsp: ENSP00000383010.2:p.Phe342Leu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1930T>C
  hgvsp: ENSP00000316377.3:p.Phe644Leu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1078T>C
  hgvsp: ENSP00000383014.3:p.Phe360Leu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1024T>C
  hgvsp: ENSP00000383011.2:p.Phe342Leu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1048T>C
  hgvsp: ENSP00000462848.1:p.Phe350Leu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1930T>C
  hgvsp: ENSP00000463864.1:p.Phe644Leu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1048T>C
  hgvsp: ENSP00000383019.1:p.Phe350Leu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.982T>C
  hgvsp: ENSP00000437817.1:p.Phe328Leu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1054T>C
  hgvsp: ENSP00000446312.1:p.Phe352Leu
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe644Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

18-3581909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581909
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581909
    reference: chr 18
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1929C>T
  hgvsp: ENST00000315677.3:c.1929C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1047C>T
  hgvsp: ENST00000581699.1:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.999C>T
  hgvsp: ENST00000400149.3:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1023C>T
  hgvsp: ENST00000400145.2:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.981C>T
  hgvsp: ENST00000534970.1:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1929C>T
  hgvsp: ENST00000584874.1:c.1929C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1047C>T
  hgvsp: ENST00000400155.1:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1053C>T
  hgvsp: ENST00000539435.1:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1023C>T
  hgvsp: ENST00000400147.2:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1077C>T
  hgvsp: ENST00000400150.3:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1929C>T
  hgvsp: ENST00000581527.1:c.1929C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1929C>T
  hgvsp: ENST00000515196.2:c.1929C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His643His
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

18-3581912-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581912
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581912
    reference: chr 18
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1020C>A
  hgvsp: ENSP00000383010.2:p.Asp340Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1044C>A
  hgvsp: ENSP00000383019.1:p.Asp348Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1044C>A
  hgvsp: ENSP00000462848.1:p.Asp348Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1926C>A
  hgvsp: ENSP00000462882.1:p.Asp642Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.978C>A
  hgvsp: ENSP00000437817.1:p.Asp326Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1926C>A
  hgvsp: ENSP00000316377.3:p.Asp642Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.996C>A
  hgvsp: ENSP00000383013.3:p.Asp332Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1020C>A
  hgvsp: ENSP00000383011.2:p.Asp340Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1926C>A
  hgvsp: ENSP00000445973.1:p.Asp642Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1074C>A
  hgvsp: ENSP00000383014.3:p.Asp358Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1050C>A
  hgvsp: ENSP00000446312.1:p.Asp350Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1926C>A
  hgvsp: ENSP00000463864.1:p.Asp642Glu
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp642Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

18-3581916-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581916
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581916
    reference: chr 18
allele count: 26
allele frequency: 2.141574551504868e-4
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1016A>G
  hgvsp: ENSP00000383010.2:p.Lys339Arg
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.992A>G
  hgvsp: ENSP00000383013.3:p.Lys331Arg
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1922A>G
  hgvsp: ENSP00000316377.3:p.Lys641Arg
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1922A>G
  hgvsp: ENSP00000445973.1:p.Lys641Arg
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1040A>G
  hgvsp: ENSP00000462848.1:p.Lys347Arg
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.974A>G
  hgvsp: ENSP00000437817.1:p.Lys325Arg
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1922A>G
  hgvsp: ENSP00000462882.1:p.Lys641Arg
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1070A>G
  hgvsp: ENSP00000383014.3:p.Lys357Arg
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1040A>G
  hgvsp: ENSP00000383019.1:p.Lys347Arg
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1046A>G
  hgvsp: ENSP00000446312.1:p.Lys349Arg
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1922A>G
  hgvsp: ENSP00000463864.1:p.Lys641Arg
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1016A>G
  hgvsp: ENSP00000383011.2:p.Lys339Arg
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 2.25e1
  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: 5065
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 9.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
hgvs: p.Lys641Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

18-3581924-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581924
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581924
    reference: chr 18
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.984C>G
  hgvsp: ENSP00000383013.3:p.Asp328Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1032C>G
  hgvsp: ENSP00000383019.1:p.Asp344Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1914C>G
  hgvsp: ENSP00000316377.3:p.Asp638Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1914C>G
  hgvsp: ENSP00000462882.1:p.Asp638Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1038C>G
  hgvsp: ENSP00000446312.1:p.Asp346Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1062C>G
  hgvsp: ENSP00000383014.3:p.Asp354Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1914C>G
  hgvsp: ENSP00000463864.1:p.Asp638Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1008C>G
  hgvsp: ENSP00000383010.2:p.Asp336Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1032C>G
  hgvsp: ENSP00000462848.1:p.Asp344Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.966C>G
  hgvsp: ENSP00000437817.1:p.Asp322Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1008C>G
  hgvsp: ENSP00000383011.2:p.Asp336Glu
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1914C>G
  hgvsp: ENSP00000445973.1:p.Asp638Glu
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp638Glu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

18-3581930-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581930
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581930
    reference: chr 18
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1026G>A
  hgvsp: ENST00000400155.1:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.960G>A
  hgvsp: ENST00000534970.1:c.960G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1908G>A
  hgvsp: ENST00000315677.3:c.1908G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1908G>A
  hgvsp: ENST00000581527.1:c.1908G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1908G>A
  hgvsp: ENST00000584874.1:c.1908G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1032G>A
  hgvsp: ENST00000539435.1:c.1032G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1056G>A
  hgvsp: ENST00000400150.3:c.1056G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.978G>A
  hgvsp: ENST00000400149.3:c.978G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1026G>A
  hgvsp: ENST00000581699.1:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1002G>A
  hgvsp: ENST00000400145.2:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1002G>A
  hgvsp: ENST00000400147.2:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1908G>A
  hgvsp: ENST00000515196.2:c.1908G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr636Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

18-3581931-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581931
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581931
    reference: chr 18
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.1001C>T
  hgvsp: ENSP00000383010.2:p.Thr334Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1907C>T
  hgvsp: ENSP00000462882.1:p.Thr636Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1055C>T
  hgvsp: ENSP00000383014.3:p.Thr352Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1907C>T
  hgvsp: ENSP00000463864.1:p.Thr636Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.959C>T
  hgvsp: ENSP00000437817.1:p.Thr320Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1907C>T
  hgvsp: ENSP00000316377.3:p.Thr636Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1025C>T
  hgvsp: ENSP00000383019.1:p.Thr342Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1031C>T
  hgvsp: ENSP00000446312.1:p.Thr344Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.977C>T
  hgvsp: ENSP00000383013.3:p.Thr326Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1025C>T
  hgvsp: ENSP00000462848.1:p.Thr342Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.1001C>T
  hgvsp: ENSP00000383011.2:p.Thr334Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1907C>T
  hgvsp: ENSP00000445973.1:p.Thr636Met
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr636Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

18-3581938-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581938
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581938
    reference: chr 18
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1900G>A
  hgvsp: ENSP00000462882.1:p.Val634Ile
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.952G>A
  hgvsp: ENSP00000437817.1:p.Val318Ile
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.994G>A
  hgvsp: ENSP00000383010.2:p.Val332Ile
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1018G>A
  hgvsp: ENSP00000462848.1:p.Val340Ile
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.970G>A
  hgvsp: ENSP00000383013.3:p.Val324Ile
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1024G>A
  hgvsp: ENSP00000446312.1:p.Val342Ile
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1900G>A
  hgvsp: ENSP00000463864.1:p.Val634Ile
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1900G>A
  hgvsp: ENSP00000445973.1:p.Val634Ile
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.994G>A
  hgvsp: ENSP00000383011.2:p.Val332Ile
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1018G>A
  hgvsp: ENSP00000383019.1:p.Val340Ile
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1900G>A
  hgvsp: ENSP00000316377.3:p.Val634Ile
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1048G>A
  hgvsp: ENSP00000383014.3:p.Val350Ile
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4678
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val634Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

18-3581939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581939
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581939
    reference: chr 18
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1023C>T
  hgvsp: ENST00000539435.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.951C>T
  hgvsp: ENST00000534970.1:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.969C>T
  hgvsp: ENST00000400149.3:c.969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1899C>T
  hgvsp: ENST00000584874.1:c.1899C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.993C>T
  hgvsp: ENST00000400147.2:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1047C>T
  hgvsp: ENST00000400150.3:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1899C>T
  hgvsp: ENST00000515196.2:c.1899C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1899C>T
  hgvsp: ENST00000315677.3:c.1899C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.993C>T
  hgvsp: ENST00000400145.2:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1017C>T
  hgvsp: ENST00000581699.1:c.1017C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1017C>T
  hgvsp: ENST00000400155.1:c.1017C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1899C>T
  hgvsp: ENST00000581527.1:c.1899C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4992
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr633Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

18-3581953-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581953
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581953
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1003A>G
  hgvsp: ENSP00000462848.1:p.Thr335Ala
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1009A>G
  hgvsp: ENSP00000446312.1:p.Thr337Ala
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1885A>G
  hgvsp: ENSP00000462882.1:p.Thr629Ala
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1885A>G
  hgvsp: ENSP00000316377.3:p.Thr629Ala
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.937A>G
  hgvsp: ENSP00000437817.1:p.Thr313Ala
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1885A>G
  hgvsp: ENSP00000445973.1:p.Thr629Ala
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1003A>G
  hgvsp: ENSP00000383019.1:p.Thr335Ala
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.955A>G
  hgvsp: ENSP00000383013.3:p.Thr319Ala
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1885A>G
  hgvsp: ENSP00000463864.1:p.Thr629Ala
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1033A>G
  hgvsp: ENSP00000383014.3:p.Thr345Ala
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.979A>G
  hgvsp: ENSP00000383011.2:p.Thr327Ala
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.979A>G
  hgvsp: ENSP00000383010.2:p.Thr327Ala
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr629Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

18-3581954-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581954
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581954
    reference: chr 18
allele count: 3
allele frequency: 2.471128976458378e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1884G>A
  hgvsp: ENST00000584874.1:c.1884G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1884G>A
  hgvsp: ENST00000515196.2:c.1884G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1884G>A
  hgvsp: ENST00000581527.1:c.1884G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.978G>A
  hgvsp: ENST00000400147.2:c.978G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1002G>A
  hgvsp: ENST00000400155.1:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.978G>A
  hgvsp: ENST00000400145.2:c.978G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1008G>A
  hgvsp: ENST00000539435.1:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.954G>A
  hgvsp: ENST00000400149.3:c.954G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1032G>A
  hgvsp: ENST00000400150.3:c.1032G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1002G>A
  hgvsp: ENST00000581699.1:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1884G>A
  hgvsp: ENST00000315677.3:c.1884G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.936G>A
  hgvsp: ENST00000534970.1:c.936G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr628Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

18-3581955-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581955
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581955
    reference: chr 18
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1883C>T
  hgvsp: ENSP00000445973.1:p.Thr628Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.977C>T
  hgvsp: ENSP00000383010.2:p.Thr326Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1007C>T
  hgvsp: ENSP00000446312.1:p.Thr336Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1883C>T
  hgvsp: ENSP00000316377.3:p.Thr628Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1883C>T
  hgvsp: ENSP00000462882.1:p.Thr628Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.1001C>T
  hgvsp: ENSP00000383019.1:p.Thr334Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.953C>T
  hgvsp: ENSP00000383013.3:p.Thr318Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1031C>T
  hgvsp: ENSP00000383014.3:p.Thr344Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.1001C>T
  hgvsp: ENSP00000462848.1:p.Thr334Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1883C>T
  hgvsp: ENSP00000463864.1:p.Thr628Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.935C>T
  hgvsp: ENSP00000437817.1:p.Thr312Met
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.977C>T
  hgvsp: ENSP00000383011.2:p.Thr326Met
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4678
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr628Met
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

18-3581960-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581960
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581960
    reference: chr 18
allele count: 4
allele frequency: 3.294784356363876e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.948C>T
  hgvsp: ENST00000400149.3:c.948C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.930C>T
  hgvsp: ENST00000534970.1:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1002C>T
  hgvsp: ENST00000539435.1:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1878C>T
  hgvsp: ENST00000584874.1:c.1878C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.972C>T
  hgvsp: ENST00000400145.2:c.972C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.996C>T
  hgvsp: ENST00000581699.1:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1026C>T
  hgvsp: ENST00000400150.3:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.972C>T
  hgvsp: ENST00000400147.2:c.972C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1878C>T
  hgvsp: ENST00000315677.3:c.1878C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1878C>T
  hgvsp: ENST00000581527.1:c.1878C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1878C>T
  hgvsp: ENST00000515196.2:c.1878C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.996C>T
  hgvsp: ENST00000400155.1:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr626Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD

18-3581960-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581960
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581960
    reference: chr 18
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1878C>G
  hgvsp: ENST00000584874.1:c.1878C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.972C>G
  hgvsp: ENST00000400147.2:c.972C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1878C>G
  hgvsp: ENST00000515196.2:c.1878C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1878C>G
  hgvsp: ENST00000315677.3:c.1878C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.996C>G
  hgvsp: ENST00000400155.1:c.996C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.996C>G
  hgvsp: ENST00000581699.1:c.996C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.1002C>G
  hgvsp: ENST00000539435.1:c.1002C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1026C>G
  hgvsp: ENST00000400150.3:c.1026C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.930C>G
  hgvsp: ENST00000534970.1:c.930C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1878C>G
  hgvsp: ENST00000581527.1:c.1878C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.948C>G
  hgvsp: ENST00000400149.3:c.948C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.972C>G
  hgvsp: ENST00000400145.2:c.972C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr626Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

18-3581966-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581966
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581966
    reference: chr 18
allele count: 25505
allele frequency: 2.102256804206986e-1
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.996C>T
  hgvsp: ENST00000539435.1:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.966C>T
  hgvsp: ENST00000400145.2:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1872C>T
  hgvsp: ENST00000515196.2:c.1872C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.924C>T
  hgvsp: ENST00000534970.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1020C>T
  hgvsp: ENST00000400150.3:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.990C>T
  hgvsp: ENST00000581699.1:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.966C>T
  hgvsp: ENST00000400147.2:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1872C>T
  hgvsp: ENST00000315677.3:c.1872C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.942C>T
  hgvsp: ENST00000400149.3:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1872C>T
  hgvsp: ENST00000581527.1:c.1872C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1872C>T
  hgvsp: ENST00000584874.1:c.1872C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.990C>T
  hgvsp: ENST00000400155.1:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 5.75e1
  variant carriers: 1252
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 4.25e1
  variant carriers: 301
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 3.75e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 4.75e1
  variant carriers: 578
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 5.25e1
  variant carriers: 889
genotype depth: GenotypeDepth
  all individuals: 8455
  bin: 9.75e1
  variant carriers: 6798
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3523
  bin: 7.75e1
  variant carriers: 1979
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 8.75e1
  variant carriers: 1491
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 7.25e1
  variant carriers: 2101
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 9.25e1
  variant carriers: 1240
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 6.75e1
  variant carriers: 1872
genotype quality: GenotypeQuality
hgvs: p.Thr624Thr
num of homozygotes: 3225
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

18-3581966-GGTGGCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581966
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581960
    reference: chr 18
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1866_1871delTGCCAC
  hgvsp: ENSP00000463864.1:p.Ala623_Thr624del
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1014_1019delTGCCAC
  hgvsp: ENSP00000383014.3:p.Ala339_Thr340del
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.960_965delTGCCAC
  hgvsp: ENSP00000383010.2:p.Ala321_Thr322del
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.984_989delTGCCAC
  hgvsp: ENSP00000383019.1:p.Ala329_Thr330del
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.984_989delTGCCAC
  hgvsp: ENSP00000462848.1:p.Ala329_Thr330del
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1866_1871delTGCCAC
  hgvsp: ENSP00000445973.1:p.Ala623_Thr624del
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1866_1871delTGCCAC
  hgvsp: ENSP00000316377.3:p.Ala623_Thr624del
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.918_923delTGCCAC
  hgvsp: ENSP00000437817.1:p.Ala307_Thr308del
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.990_995delTGCCAC
  hgvsp: ENSP00000446312.1:p.Ala331_Thr332del
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.960_965delTGCCAC
  hgvsp: ENSP00000383011.2:p.Ala321_Thr322del
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1866_1871delTGCCAC
  hgvsp: ENSP00000462882.1:p.Ala623_Thr624del
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.936_941delTGCCAC
  hgvsp: ENSP00000383013.3:p.Ala313_Thr314del
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8455
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala623_Thr624del
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: GGTGGCA
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum

18-3581970-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581970
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581970
    reference: chr 18
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.962C>A
  hgvsp: ENSP00000383010.2:p.Ala321Asp
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.992C>A
  hgvsp: ENSP00000446312.1:p.Ala331Asp
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.920C>A
  hgvsp: ENSP00000437817.1:p.Ala307Asp
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.962C>A
  hgvsp: ENSP00000383011.2:p.Ala321Asp
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1868C>A
  hgvsp: ENSP00000445973.1:p.Ala623Asp
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1868C>A
  hgvsp: ENSP00000462882.1:p.Ala623Asp
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.938C>A
  hgvsp: ENSP00000383013.3:p.Ala313Asp
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1016C>A
  hgvsp: ENSP00000383014.3:p.Ala339Asp
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1868C>A
  hgvsp: ENSP00000316377.3:p.Ala623Asp
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.986C>A
  hgvsp: ENSP00000462848.1:p.Ala329Asp
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.986C>A
  hgvsp: ENSP00000383019.1:p.Ala329Asp
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1868C>A
  hgvsp: ENSP00000463864.1:p.Ala623Asp
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6005
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala623Asp
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

18-3581974-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581974
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581974
    reference: chr 18
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.988A>T
  hgvsp: ENSP00000446312.1:p.Thr330Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.958A>T
  hgvsp: ENSP00000383010.2:p.Thr320Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1864A>T
  hgvsp: ENSP00000463864.1:p.Thr622Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.934A>T
  hgvsp: ENSP00000383013.3:p.Thr312Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1864A>T
  hgvsp: ENSP00000316377.3:p.Thr622Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1864A>T
  hgvsp: ENSP00000462882.1:p.Thr622Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1864A>T
  hgvsp: ENSP00000445973.1:p.Thr622Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.958A>T
  hgvsp: ENSP00000383011.2:p.Thr320Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.982A>T
  hgvsp: ENSP00000383019.1:p.Thr328Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.916A>T
  hgvsp: ENSP00000437817.1:p.Thr306Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.982A>T
  hgvsp: ENSP00000462848.1:p.Thr328Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1012A>T
  hgvsp: ENSP00000383014.3:p.Thr338Ser
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr622Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-3581983-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581983
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581983
    reference: chr 18
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1855G>A
  hgvsp: ENSP00000316377.3:p.Gly619Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.949G>A
  hgvsp: ENSP00000383011.2:p.Gly317Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.973G>A
  hgvsp: ENSP00000383019.1:p.Gly325Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1855G>A
  hgvsp: ENSP00000463864.1:p.Gly619Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1855G>A
  hgvsp: ENSP00000462882.1:p.Gly619Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1855G>A
  hgvsp: ENSP00000445973.1:p.Gly619Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.907G>A
  hgvsp: ENSP00000437817.1:p.Gly303Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.973G>A
  hgvsp: ENSP00000462848.1:p.Gly325Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.979G>A
  hgvsp: ENSP00000446312.1:p.Gly327Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.949G>A
  hgvsp: ENSP00000383010.2:p.Gly317Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.925G>A
  hgvsp: ENSP00000383013.3:p.Gly309Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1003G>A
  hgvsp: ENSP00000383014.3:p.Gly335Ser
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly619Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

18-3581985-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3581985
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3581985
    reference: chr 18
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.947T>C
  hgvsp: ENSP00000383010.2:p.Met316Thr
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.977T>C
  hgvsp: ENSP00000446312.1:p.Met326Thr
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.971T>C
  hgvsp: ENSP00000383019.1:p.Met324Thr
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1853T>C
  hgvsp: ENSP00000463864.1:p.Met618Thr
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.1001T>C
  hgvsp: ENSP00000383014.3:p.Met334Thr
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.923T>C
  hgvsp: ENSP00000383013.3:p.Met308Thr
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.905T>C
  hgvsp: ENSP00000437817.1:p.Met302Thr
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1853T>C
  hgvsp: ENSP00000462882.1:p.Met618Thr
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.971T>C
  hgvsp: ENSP00000462848.1:p.Met324Thr
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.947T>C
  hgvsp: ENSP00000383011.2:p.Met316Thr
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1853T>C
  hgvsp: ENSP00000316377.3:p.Met618Thr
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1853T>C
  hgvsp: ENSP00000445973.1:p.Met618Thr
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met618Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

18-3582017-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582017
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582017
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1821C>T
  hgvsp: ENST00000315677.3:c.1821C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.891C>T
  hgvsp: ENST00000400149.3:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.939C>T
  hgvsp: ENST00000581699.1:c.939C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1821C>T
  hgvsp: ENST00000581527.1:c.1821C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1821C>T
  hgvsp: ENST00000584874.1:c.1821C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.915C>T
  hgvsp: ENST00000400145.2:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.969C>T
  hgvsp: ENST00000400150.3:c.969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.939C>T
  hgvsp: ENST00000400155.1:c.939C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1821C>T
  hgvsp: ENST00000515196.2:c.1821C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.945C>T
  hgvsp: ENST00000539435.1:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.915C>T
  hgvsp: ENST00000400147.2:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.873C>T
  hgvsp: ENST00000534970.1:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5993
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn607Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

18-3582029-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582029
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582029
    reference: chr 18
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1809C>T
  hgvsp: ENST00000515196.2:c.1809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.927C>T
  hgvsp: ENST00000581699.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1809C>T
  hgvsp: ENST00000315677.3:c.1809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.903C>T
  hgvsp: ENST00000400145.2:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.957C>T
  hgvsp: ENST00000400150.3:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.933C>T
  hgvsp: ENST00000539435.1:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1809C>T
  hgvsp: ENST00000584874.1:c.1809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.927C>T
  hgvsp: ENST00000400155.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.879C>T
  hgvsp: ENST00000400149.3:c.879C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1809C>T
  hgvsp: ENST00000581527.1:c.1809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.903C>T
  hgvsp: ENST00000400147.2:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.861C>T
  hgvsp: ENST00000534970.1:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile603Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

18-3582035-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582035
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582035
    reference: chr 18
allele count: 6
allele frequency: 4.942013705851344e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.921C>T
  hgvsp: ENST00000581699.1:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.951C>T
  hgvsp: ENST00000400150.3:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.873C>T
  hgvsp: ENST00000400149.3:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.855C>T
  hgvsp: ENST00000534970.1:c.855C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1803C>T
  hgvsp: ENST00000584874.1:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.927C>T
  hgvsp: ENST00000539435.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.897C>T
  hgvsp: ENST00000400145.2:c.897C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1803C>T
  hgvsp: ENST00000315677.3:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.921C>T
  hgvsp: ENST00000400155.1:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.897C>T
  hgvsp: ENST00000400147.2:c.897C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1803C>T
  hgvsp: ENST00000581527.1:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1803C>T
  hgvsp: ENST00000515196.2:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4974
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5993
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5844
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala601Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-3582041-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582041
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582041
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1797G>T
  hgvsp: ENST00000315677.3:c.1797G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.891G>T
  hgvsp: ENST00000400147.2:c.891G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.867G>T
  hgvsp: ENST00000400149.3:c.867G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1797G>T
  hgvsp: ENST00000584874.1:c.1797G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.945G>T
  hgvsp: ENST00000400150.3:c.945G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.915G>T
  hgvsp: ENST00000581699.1:c.915G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.921G>T
  hgvsp: ENST00000539435.1:c.921G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.891G>T
  hgvsp: ENST00000400145.2:c.891G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.849G>T
  hgvsp: ENST00000534970.1:c.849G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1797G>T
  hgvsp: ENST00000515196.2:c.1797G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.915G>T
  hgvsp: ENST00000400155.1:c.915G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1797G>T
  hgvsp: ENST00000581527.1:c.1797G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4032
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu599Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ

18-3582068-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582068
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582068
    reference: chr 18
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.918C>T
  hgvsp: ENST00000400150.3:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1770C>T
  hgvsp: ENST00000584874.1:c.1770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.888C>T
  hgvsp: ENST00000400155.1:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.864C>T
  hgvsp: ENST00000400147.2:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.888C>T
  hgvsp: ENST00000581699.1:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.894C>T
  hgvsp: ENST00000539435.1:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.840C>T
  hgvsp: ENST00000400149.3:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.864C>T
  hgvsp: ENST00000400145.2:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.822C>T
  hgvsp: ENST00000534970.1:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1770C>T
  hgvsp: ENST00000315677.3:c.1770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1770C>T
  hgvsp: ENST00000581527.1:c.1770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1770C>T
  hgvsp: ENST00000515196.2:c.1770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr590Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

18-3582086-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582086
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582086
    reference: chr 18
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.870T>C
  hgvsp: ENST00000400155.1:c.870T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1752T>C
  hgvsp: ENST00000315677.3:c.1752T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1752T>C
  hgvsp: ENST00000584874.1:c.1752T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.876T>C
  hgvsp: ENST00000539435.1:c.876T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.870T>C
  hgvsp: ENST00000581699.1:c.870T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1752T>C
  hgvsp: ENST00000581527.1:c.1752T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.822T>C
  hgvsp: ENST00000400149.3:c.822T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.846T>C
  hgvsp: ENST00000400145.2:c.846T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.846T>C
  hgvsp: ENST00000400147.2:c.846T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.900T>C
  hgvsp: ENST00000400150.3:c.900T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1752T>C
  hgvsp: ENST00000515196.2:c.1752T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.804T>C
  hgvsp: ENST00000534970.1:c.804T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser584Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

18-3582101-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582101
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582101
    reference: chr 18
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.855T>C
  hgvsp: ENST00000581699.1:c.855T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.831T>C
  hgvsp: ENST00000400145.2:c.831T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.831T>C
  hgvsp: ENST00000400147.2:c.831T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1737T>C
  hgvsp: ENST00000315677.3:c.1737T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.861T>C
  hgvsp: ENST00000539435.1:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1737T>C
  hgvsp: ENST00000584874.1:c.1737T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.885T>C
  hgvsp: ENST00000400150.3:c.885T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.789T>C
  hgvsp: ENST00000534970.1:c.789T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1737T>C
  hgvsp: ENST00000515196.2:c.1737T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.807T>C
  hgvsp: ENST00000400149.3:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1737T>C
  hgvsp: ENST00000581527.1:c.1737T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.855T>C
  hgvsp: ENST00000400155.1:c.855T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp579Asp
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

18-3582104-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582104
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582104
    reference: chr 18
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.786A>G
  hgvsp: ENST00000534970.1:c.786A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.828A>G
  hgvsp: ENST00000400147.2:c.828A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1734A>G
  hgvsp: ENST00000315677.3:c.1734A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.852A>G
  hgvsp: ENST00000400155.1:c.852A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.882A>G
  hgvsp: ENST00000400150.3:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.858A>G
  hgvsp: ENST00000539435.1:c.858A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1734A>G
  hgvsp: ENST00000584874.1:c.1734A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.852A>G
  hgvsp: ENST00000581699.1:c.852A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.804A>G
  hgvsp: ENST00000400149.3:c.804A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1734A>G
  hgvsp: ENST00000515196.2:c.1734A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1734A>G
  hgvsp: ENST00000581527.1:c.1734A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.828A>G
  hgvsp: ENST00000400145.2:c.828A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly578Gly
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

18-3582108-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582108
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582108
    reference: chr 18
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.848G>A
  hgvsp: ENSP00000383019.1:p.Arg283Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1730G>A
  hgvsp: ENSP00000445973.1:p.Arg577Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.824G>A
  hgvsp: ENSP00000383011.2:p.Arg275Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.848G>A
  hgvsp: ENSP00000462848.1:p.Arg283Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1730G>A
  hgvsp: ENSP00000462882.1:p.Arg577Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.878G>A
  hgvsp: ENSP00000383014.3:p.Arg293Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.824G>A
  hgvsp: ENSP00000383010.2:p.Arg275Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.854G>A
  hgvsp: ENSP00000446312.1:p.Arg285Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1730G>A
  hgvsp: ENSP00000316377.3:p.Arg577Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.800G>A
  hgvsp: ENSP00000383013.3:p.Arg267Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1730G>A
  hgvsp: ENSP00000463864.1:p.Arg577Gln
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.782G>A
  hgvsp: ENSP00000437817.1:p.Arg261Gln
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg577Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

18-3582110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582110
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582110
    reference: chr 18
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.822G>A
  hgvsp: ENST00000400147.2:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.846G>A
  hgvsp: ENST00000400155.1:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.852G>A
  hgvsp: ENST00000539435.1:c.852G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1728G>A
  hgvsp: ENST00000515196.2:c.1728G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.876G>A
  hgvsp: ENST00000400150.3:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1728G>A
  hgvsp: ENST00000315677.3:c.1728G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.780G>A
  hgvsp: ENST00000534970.1:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1728G>A
  hgvsp: ENST00000584874.1:c.1728G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.822G>A
  hgvsp: ENST00000400145.2:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.846G>A
  hgvsp: ENST00000581699.1:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1728G>A
  hgvsp: ENST00000581527.1:c.1728G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.798G>A
  hgvsp: ENST00000400149.3:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4066
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln576Gln
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: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

18-3582115-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582115
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582115
    reference: chr 18
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.817G>A
  hgvsp: ENSP00000383010.2:p.Gly273Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1723G>A
  hgvsp: ENSP00000463864.1:p.Gly575Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.817G>A
  hgvsp: ENSP00000383011.2:p.Gly273Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.847G>A
  hgvsp: ENSP00000446312.1:p.Gly283Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.841G>A
  hgvsp: ENSP00000462848.1:p.Gly281Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.841G>A
  hgvsp: ENSP00000383019.1:p.Gly281Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.793G>A
  hgvsp: ENSP00000383013.3:p.Gly265Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1723G>A
  hgvsp: ENSP00000316377.3:p.Gly575Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.775G>A
  hgvsp: ENSP00000437817.1:p.Gly259Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1723G>A
  hgvsp: ENSP00000462882.1:p.Gly575Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.871G>A
  hgvsp: ENSP00000383014.3:p.Gly291Ser
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1723G>A
  hgvsp: ENSP00000445973.1:p.Gly575Ser
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4066
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly575Ser
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

18-3582122-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582122
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582122
    reference: chr 18
allele count: 20
allele frequency: 1.647283629295292e-4
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.834C>T
  hgvsp: ENST00000581699.1:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1716C>T
  hgvsp: ENST00000581527.1:c.1716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1716C>T
  hgvsp: ENST00000515196.2:c.1716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.864C>T
  hgvsp: ENST00000400150.3:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.810C>T
  hgvsp: ENST00000400145.2:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1716C>T
  hgvsp: ENST00000584874.1:c.1716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.768C>T
  hgvsp: ENST00000534970.1:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.786C>T
  hgvsp: ENST00000400149.3:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.840C>T
  hgvsp: ENST00000539435.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.834C>T
  hgvsp: ENST00000400155.1:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1716C>T
  hgvsp: ENST00000315677.3:c.1716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.810C>T
  hgvsp: ENST00000400147.2:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp572Asp
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

18-3582128-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3582128
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 3582128
    reference: chr 18
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000316377
  ensembl transcript: ENST00000315677
  gene symbol: DLGAP1
  hgvsc: ENST00000315677.3:c.1710C>T
  hgvsp: ENST00000315677.3:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462848
  ensembl transcript: ENST00000581699
  gene symbol: DLGAP1
  hgvsc: ENST00000581699.1:c.828C>T
  hgvsp: ENST00000581699.1:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383019
  ensembl transcript: ENST00000400155
  gene symbol: DLGAP1
  hgvsc: ENST00000400155.1:c.828C>T
  hgvsp: ENST00000400155.1:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000445973
  ensembl transcript: ENST00000515196
  gene symbol: DLGAP1
  hgvsc: ENST00000515196.2:c.1710C>T
  hgvsp: ENST00000515196.2:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000462882
  ensembl transcript: ENST00000584874
  gene symbol: DLGAP1
  hgvsc: ENST00000584874.1:c.1710C>T
  hgvsp: ENST00000584874.1:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383013
  ensembl transcript: ENST00000400149
  gene symbol: DLGAP1
  hgvsc: ENST00000400149.3:c.780C>T
  hgvsp: ENST00000400149.3:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000463864
  ensembl transcript: ENST00000581527
  gene symbol: DLGAP1
  hgvsc: ENST00000581527.1:c.1710C>T
  hgvsp: ENST00000581527.1:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383011
  ensembl transcript: ENST00000400147
  gene symbol: DLGAP1
  hgvsc: ENST00000400147.2:c.804C>T
  hgvsp: ENST00000400147.2:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000446312
  ensembl transcript: ENST00000539435
  gene symbol: DLGAP1
  hgvsc: ENST00000539435.1:c.834C>T
  hgvsp: ENST00000539435.1:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000437817
  ensembl transcript: ENST00000534970
  gene symbol: DLGAP1
  hgvsc: ENST00000534970.1:c.762C>T
  hgvsp: ENST00000534970.1:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383010
  ensembl transcript: ENST00000400145
  gene symbol: DLGAP1
  hgvsc: ENST00000400145.2:c.804C>T
  hgvsp: ENST00000400145.2:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170579
  ensembl protein: ENSP00000383014
  ensembl transcript: ENST00000400150
  gene symbol: DLGAP1
  hgvsc: ENST00000400150.3:c.858C>T
  hgvsp: ENST00000400150.3:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr570Tyr
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 2279
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3389
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 591
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2064
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3639
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3490
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7660
bin: 6.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 3437
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34907
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3391
bin: 8.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.987e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.992314e6

VQSLOD
type: SiteQuality
SIO_000300: 5.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.676e0

MQRankSum
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 1.478e1

FS
type: SiteQuality
SIO_000300: 1.921e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.576e0

GenotypeDepth
all individuals: 591
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 660
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7757
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3389
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 34907
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7661
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3640
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2064
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3437
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3490
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.987e1

DP
type: SiteQuality
SIO_000300: 2.992552e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.75e-1

FS
type: SiteQuality
SIO_000300: 4.611e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.075e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 7.4e0

GenotypeDepth
all individuals: 3389
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 837
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4727
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3490
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3638
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3437
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7660
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3391
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2108
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2064
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34909
bin: 9.75e1
variant carriers: 3

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.17e-1

FS
type: SiteQuality
SIO_000300: 1.139e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e-1

QD
type: SiteQuality
SIO_000300: 1.193e1

MQRankSum
type: SiteQuality
SIO_000300: 6.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

DP
type: SiteQuality
SIO_000300: 2.992422e6

GenotypeDepth
all individuals: 1245
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 837
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1706
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7663
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3490
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2064
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3437
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3391
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34908
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3638
bin: 6.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.03e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 2.992488e6

VQSLOD
type: SiteQuality
SIO_000300: 2.83e0

MQ
type: SiteQuality
SIO_000300: 5.994e1

QD
type: SiteQuality
SIO_000300: 1.203e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

GenotypeDepth
all individuals: 6602
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 591
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 968
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4726
bin: 5.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3639
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7658
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3490
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 34907
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3437
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2064
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-1

FS
type: SiteQuality
SIO_000300: 2.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 2.99223e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.335e0

QD
type: SiteQuality
SIO_000300: 1.12e1

VQSLOD
type: SiteQuality
SIO_000300: 4.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

GenotypeDepth
all individuals: 4003
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 591
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3389
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7917
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Other
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African
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ClippingRankSum
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QD
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BaseQRankSum
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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East Asian
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Other
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Latino
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African
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European (Finnish)
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FS
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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DP
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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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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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African
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Other
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Latino
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DP
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FS
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MQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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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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Other
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African
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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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European (Finnish)
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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VQSLOD
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FS
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BaseQRankSum
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MQ
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DP
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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 (Finnish)
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African
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East Asian
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Latino
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Other
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European (Non-Finnish)
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South Asian
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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Latino
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South Asian
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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DP
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MQRankSum
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MQ
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FS
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VQSLOD
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QD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.998980173370527e-5
allele num: 66678
num of homozygotes: 0

Other
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num of homozygotes: 0

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

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

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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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: 3.8e-2

ClippingRankSum
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QD
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DP
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VQSLOD
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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SIO_000300: 4.6e-3

BaseQRankSum
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SIO_000300: 3.27e-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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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 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: 0.0e0
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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QD
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FS
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ClippingRankSum
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VQSLOD
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MQ
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BaseQRankSum
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SIO_000300: 3.02e0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele num: 904
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European (Finnish)
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allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

East Asian
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VQSLOD
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SIO_000300: 1.96e0

MQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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FS
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QD
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InbreedingCoeff
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SIO_000300: 1.1e-3

BaseQRankSum
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SIO_000300: 8.39e-1

MQ
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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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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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bin: 8.75e1
variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 904
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

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

African
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allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: 1.1e-3

ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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MQ
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QD
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FS
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VQSLOD
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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: 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 frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 65896
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South Asian
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Other
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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FS
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DP
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MQ
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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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variant carriers: 0

Other
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num of homozygotes: 0

African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Latino
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East Asian
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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DP
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InbreedingCoeff
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MQ
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ClippingRankSum
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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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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

European (Non-Finnish)
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African
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Other
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Latino
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East Asian
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South Asian
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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QD
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MQRankSum
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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: 2

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 1.297353399065905e-4
allele num: 15416
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65976
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
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ReadPosRankSum
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SIO_000300: 5.3e-1

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 2.95e-1

FS
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DP
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MQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: 1.03e0

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

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
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variant carriers: 0

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

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: 6.45244547683572e-5
allele num: 15498
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66010
num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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FS
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VQSLOD
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QD
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SIO_000300: 1.418e1

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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variant carriers: 0

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

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

South Asian
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allele frequency: 6.341958396752917e-5
allele num: 15768
num of homozygotes: 0

African
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allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
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SIO_000300: 4.3e-2

InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: -1.1e-2

MQ
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SIO_000300: 5.945e1

DP
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FS
type: SiteQuality
SIO_000300: 5.273e0

QD
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SIO_000300: 1.435e1

GenotypeDepth
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variant carriers: 4

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: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 4
allele frequency: 3.896356906292616e-4
allele num: 10266
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509433962264151e-5
allele num: 66250
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.022e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
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SIO_000300: 3.5e-3

FS
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SIO_000300: 3.752e0

DP
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BaseQRankSum
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SIO_000300: 1.15e0

MQRankSum
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SIO_000300: 8.49e-1

ClippingRankSum
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SIO_000300: -3.76e-1

QD
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SIO_000300: 1.271e1

VQSLOD
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SIO_000300: 1.58e0

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: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 66416
num of homozygotes: 0

Latino
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allele frequency: 6.91085003455425e-4
allele num: 11576
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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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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FS
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DP
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ReadPosRankSum
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QD
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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

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: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
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allele num: 66478
num of homozygotes: 0

European (Finnish)
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African
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Other
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South Asian
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ReadPosRankSum
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

Other
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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East Asian
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ReadPosRankSum
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FS
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MQRankSum
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QD
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DP
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BaseQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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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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Other
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Latino
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European (Non-Finnish)
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European (Finnish)
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South Asian
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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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DP
type: SiteQuality
SIO_000300: 3.620976e6

MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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SIO_000300: -2.96e-1

MQ
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SIO_000300: 5.92e1

InbreedingCoeff
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SIO_000300: -1.0e-4

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 8.75e1
variant carriers: 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
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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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allele frequency: 2.851054890309415e-4
allele num: 66642
num of homozygotes: 0

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

Latino
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allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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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

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.983e1

QD
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BaseQRankSum
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SIO_000300: 2.61e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
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ClippingRankSum
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SIO_000300: -6.55e-1

FS
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SIO_000300: 5.24e-1

MQRankSum
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SIO_000300: -6.7e-2

ReadPosRankSum
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SIO_000300: 9.28e-1

DP
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SIO_000300: 3.622293e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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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: 10406
num of homozygotes: 0

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

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

South Asian
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allele frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

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

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

MQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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FS
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ClippingRankSum
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MQ
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SIO_000300: 5.963e1

BaseQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

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

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

Latino
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allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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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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num of homozygotes: 0

European (Non-Finnish)
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Other
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European (Finnish)
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African
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East Asian
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Latino
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DP
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FS
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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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QD
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Finnish)
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num of homozygotes: 0

South Asian
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Latino
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African
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East Asian
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Other
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European (Non-Finnish)
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allele num: 66716
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MQ
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FS
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InbreedingCoeff
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DP
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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Other
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Latino
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MQ
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QD
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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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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num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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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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num of homozygotes: 0

Latino
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African
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East Asian
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European (Non-Finnish)
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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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QD
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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variant carriers: 26

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

GenotypeDepth
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GenotypeDepth
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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: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 4.495190146543199e-5
allele num: 66738
num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

African
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Other
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Latino
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VQSLOD
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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DP
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BaseQRankSum
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 2.25e1
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
allele num: 11578
num of homozygotes: 0

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

Other
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South Asian
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Latino
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African
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East Asian
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European (Non-Finnish)
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BaseQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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DP
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VQSLOD
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QD
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ReadPosRankSum
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MQ
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

African
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num of homozygotes: 0

East Asian
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Other
type: Population
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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MQ
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VQSLOD
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QD
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FS
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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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

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66738
num of homozygotes: 0

African
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allele num: 10404
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European (Finnish)
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South Asian
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Latino
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East Asian
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MQ
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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FS
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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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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num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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South Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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QD
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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SIO_000300: 2.0e-4

MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 1758

GenotypeDepth
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GenotypeDepth
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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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allele count: 222
allele frequency: 2.444933920704846e-1
allele num: 908
num of homozygotes: 26

European (Non-Finnish)
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allele frequency: 2.744953963350628e-1
allele num: 66686
num of homozygotes: 2528

African
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East Asian
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allele frequency: 1.965317919075144e-3
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Latino
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allele frequency: 1.852620653866113e-1
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European (Finnish)
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allele frequency: 2.757419745608722e-1
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South Asian
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allele frequency: 1.448818897637795e-1
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ReadPosRankSum
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SIO_000300: 4.5e-1

ClippingRankSum
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FS
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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SIO_000300: 4.96e-2

VQSLOD
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DP
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BaseQRankSum
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SIO_000300: 1.4e0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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Other
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East Asian
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Latino
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African
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South Asian
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DP
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SIO_000300: 4.079454e6

QD
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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SIO_000300: 1.4e0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

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

European (Finnish)
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Other
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East Asian
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South Asian
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FS
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InbreedingCoeff
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DP
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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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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
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African
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South Asian
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East Asian
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Latino
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allele frequency: 0.0e0
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Other
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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SIO_000300: 8.22e-1

ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 5.25e1
variant carriers: 0

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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

African
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allele frequency: 0.0e0
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66736
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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VQSLOD
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MQ
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QD
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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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 (Non-Finnish)
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allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

South Asian
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Other
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African
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allele frequency: 0.0e0
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Latino
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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

MQ
type: SiteQuality
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QD
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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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: 6

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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African
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allele count: 0
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Latino
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allele num: 11578
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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allele num: 16512
num of homozygotes: 0

East Asian
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DP
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FS
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VQSLOD
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MQ
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MQRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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num of homozygotes: 0

African
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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European (Finnish)
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ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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QD
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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Other
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African
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MQRankSum
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MQ
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FS
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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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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Latino
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BaseQRankSum
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DP
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FS
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QD
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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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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African
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European (Non-Finnish)
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VQSLOD
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FS
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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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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African
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Latino
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European (Non-Finnish)
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East Asian
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MQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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QD
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InbreedingCoeff
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MQ
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BaseQRankSum
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GenotypeDepth
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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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Latino
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South Asian
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African
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East Asian
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European (Non-Finnish)
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MQ
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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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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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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South Asian
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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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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African
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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FS
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ClippingRankSum
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DP
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BaseQRankSum
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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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South Asian
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African
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European (Non-Finnish)
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East Asian
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Latino
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QD
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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