2-183094859-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183094859
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183094859
    reference: chr 2
allele count: 54
allele frequency: 4.47427293064877e-4
allele num: 120690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.549C>T
  hgvsp: ENST00000351439.5:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.567C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.597C>T
  hgvsp: ENST00000358139.2:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.597C>T
  hgvsp: ENST00000410103.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.597C>T
  hgvsp: ENST00000331935.6:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.549C>T
  hgvsp: ENST00000409365.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.285C>T
  hgvsp: ENST00000536095.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.597C>T
  hgvsp: ENST00000456212.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.495C>T
  hgvsp: ENST00000346717.4:c.495C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.597C>T
  hgvsp: ENST00000435564.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10217
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15675
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23064
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys199Cys
num of homozygotes: 2
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/2-183094881-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183094881
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183094881
    reference: chr 2
allele count: 1
allele frequency: 8.783487044356609e-6
allele num: 113850
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.553-8T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.481-8T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.535-8T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.583-8T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.535-8T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.583-8T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.271-8T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.583-8T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.583-8T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.583-8T>G
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7565
  bin: 6.75e1
  variant carriers: 0
hgvs: c.583-8T>G
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

2-183094908-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183094908
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183094908
    reference: chr 2
allele count: 25
allele frequency: 2.539102173471461e-4
allele num: 98460
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.583-35G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.583-35G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.535-35G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.481-35G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.271-35G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.553-35G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.583-35G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.583-35G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.535-35G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.583-35G>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8264
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22281
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1651
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-183094908-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183094908
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183094907
    reference: chr 2
allele count: 10
allele frequency: 1.015640869388584e-4
allele num: 98460
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.583-36delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.481-36delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.535-36delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.583-36delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.583-36delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.583-36delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.553-36delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.271-36delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.535-36delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.583-36delT
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22281
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8264
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2334
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5675
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: CA
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-183094908-CAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183094908
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183094906
    reference: chr 2
allele count: 2
allele frequency: 2.031281738777168e-5
allele num: 98460
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8342
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17573
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2334
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1651
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5416
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 13118
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9918
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 53864
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5912
  num of homozygotes: 0
population: African
population: East Asian
population: Other
reference allele: CAA
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-183094914-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183094914
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183094914
    reference: chr 2
allele count: 2
allele frequency: 2.065432914738929e-5
allele num: 96832
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.583-41T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.583-41T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.583-41T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.271-41T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.583-41T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.553-41T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.481-41T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.535-41T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.583-41T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.535-41T>G
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2095
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9057
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2469
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

2-183094915-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183094915
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183094915
    reference: chr 2
allele count: 9
allele frequency: 9.314263241777575e-5
allele num: 96626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.481-42C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.583-42C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.535-42C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.535-42C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.583-42C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.553-42C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.583-42C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.583-42C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.583-42C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.271-42C>T
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14551
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9800
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21542
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 9.75e1
  variant carriers: 9
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

2-183094919-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183094919
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183094919
    reference: chr 2
allele count: 1
allele frequency: 1.061683830555261e-5
allele num: 94190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.583-46A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.553-46A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.583-46A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.535-46A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.481-46A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.583-46A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.583-46A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.535-46A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.271-46A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.583-46A>G
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20610
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1963
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3314
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

2-183095691-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095691
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095691
    reference: chr 2
allele count: 1
allele frequency: 8.593723144615173e-6
allele num: 116364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.270+51T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.582+51T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.582+51T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.534+51T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.582+51T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.552+51T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.534+51T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.582+51T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.582+51T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.480+51T>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4225
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/2-183095692-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095692
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095692
    reference: chr 2
allele count: 1
allele frequency: 8.60037497634897e-6
allele num: 116274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.582+50G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.534+50G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.552+50G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.582+50G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.582+50G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.582+50G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.582+50G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.534+50G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.480+50G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.270+50G>T
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

2-183095704-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095704
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095704
    reference: chr 2
allele count: 21
allele frequency: 1.801801801801802e-4
allele num: 116550
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.582+38T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.582+38T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.552+38T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.480+38T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.582+38T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.534+38T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.582+38T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.534+38T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.270+38T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.582+38T>C
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/2-183095714-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095714
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095714
    reference: chr 2
allele count: 1
allele frequency: 8.557833841098141e-6
allele num: 116852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.534+28G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.582+28G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.582+28G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.582+28G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.552+28G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.582+28G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.270+28G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.534+28G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.582+28G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.480+28G>T
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

2-183095749-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095749
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095749
    reference: chr 2
allele count: 41
allele frequency: 3.426661094860008e-4
allele num: 119650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.545G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.527G>A
  hgvsp: ENSP00000309269.9:p.Arg176His
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.263G>A
  hgvsp: ENSP00000439938.1:p.Arg88His
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.575G>A
  hgvsp: ENSP00000410309.1:p.Arg192His
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.575G>A
  hgvsp: ENSP00000331574.6:p.Arg192His
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.575G>A
  hgvsp: ENSP00000387037.1:p.Arg192His
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.473G>A
  hgvsp: ENSP00000329112.4:p.Arg158His
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.575G>A
  hgvsp: ENSP00000350858.2:p.Arg192His
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.575G>A
  hgvsp: ENSP00000408874.1:p.Arg192His
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.527G>A
  hgvsp: ENSP00000386767.1:p.Arg176His
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg192His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

2-183095750-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095750
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095750
    reference: chr 2
allele count: 3
allele frequency: 2.503421342501419e-5
allele num: 119836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.574C>T
  hgvsp: ENSP00000408874.1:p.Arg192Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.526C>T
  hgvsp: ENSP00000386767.1:p.Arg176Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.544C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.574C>T
  hgvsp: ENSP00000331574.6:p.Arg192Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.526C>T
  hgvsp: ENSP00000309269.9:p.Arg176Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.262C>T
  hgvsp: ENSP00000439938.1:p.Arg88Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.574C>T
  hgvsp: ENSP00000410309.1:p.Arg192Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.574C>T
  hgvsp: ENSP00000387037.1:p.Arg192Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.574C>T
  hgvsp: ENSP00000350858.2:p.Arg192Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.472C>T
  hgvsp: ENSP00000329112.4:p.Arg158Cys
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg192Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

2-183095756-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095756
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095756
    reference: chr 2
allele count: 1
allele frequency: 8.319329129299013e-6
allele num: 120202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.520A>C
  hgvsp: ENSP00000309269.9:p.Ile174Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.568A>C
  hgvsp: ENSP00000410309.1:p.Ile190Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.568A>C
  hgvsp: ENSP00000331574.6:p.Ile190Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.538A>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.520A>C
  hgvsp: ENSP00000386767.1:p.Ile174Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.568A>C
  hgvsp: ENSP00000408874.1:p.Ile190Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.256A>C
  hgvsp: ENSP00000439938.1:p.Ile86Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.568A>C
  hgvsp: ENSP00000387037.1:p.Ile190Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.568A>C
  hgvsp: ENSP00000350858.2:p.Ile190Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.466A>C
  hgvsp: ENSP00000329112.4:p.Ile156Leu
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile190Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

2-183095759-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095759
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095759
    reference: chr 2
allele count: 1
allele frequency: 8.306889734345666e-6
allele num: 120382
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.565C>G
  hgvsp: ENSP00000410309.1:p.Leu189Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.565C>G
  hgvsp: ENSP00000350858.2:p.Leu189Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.517C>G
  hgvsp: ENSP00000386767.1:p.Leu173Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.517C>G
  hgvsp: ENSP00000309269.9:p.Leu173Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.565C>G
  hgvsp: ENSP00000408874.1:p.Leu189Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.253C>G
  hgvsp: ENSP00000439938.1:p.Leu85Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.565C>G
  hgvsp: ENSP00000331574.6:p.Leu189Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.535C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.463C>G
  hgvsp: ENSP00000329112.4:p.Leu155Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.565C>G
  hgvsp: ENSP00000387037.1:p.Leu189Val
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu189Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-183095761-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095761
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095761
    reference: chr 2
allele count: 1
allele frequency: 8.299443937256203e-6
allele num: 120490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.515A>T
  hgvsp: ENSP00000309269.9:p.Asp172Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.563A>T
  hgvsp: ENSP00000410309.1:p.Asp188Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.515A>T
  hgvsp: ENSP00000386767.1:p.Asp172Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.461A>T
  hgvsp: ENSP00000329112.4:p.Asp154Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.563A>T
  hgvsp: ENSP00000331574.6:p.Asp188Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.533A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.251A>T
  hgvsp: ENSP00000439938.1:p.Asp84Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.563A>T
  hgvsp: ENSP00000387037.1:p.Asp188Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.563A>T
  hgvsp: ENSP00000408874.1:p.Asp188Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.563A>T
  hgvsp: ENSP00000350858.2:p.Asp188Val
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp188Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/2-183095762-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095762
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095762
    reference: chr 2
allele count: 2
allele frequency: 1.65892501658925e-5
allele num: 120560
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.562G>T
  hgvsp: ENSP00000410309.1:p.Asp188Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.562G>T
  hgvsp: ENSP00000408874.1:p.Asp188Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.532G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.562G>T
  hgvsp: ENSP00000331574.6:p.Asp188Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.514G>T
  hgvsp: ENSP00000309269.9:p.Asp172Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.514G>T
  hgvsp: ENSP00000386767.1:p.Asp172Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.250G>T
  hgvsp: ENSP00000439938.1:p.Asp84Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.562G>T
  hgvsp: ENSP00000387037.1:p.Asp188Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.460G>T
  hgvsp: ENSP00000329112.4:p.Asp154Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.562G>T
  hgvsp: ENSP00000350858.2:p.Asp188Tyr
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp188Tyr
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

2-183095775-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095775
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095775
    reference: chr 2
allele count: 3
allele frequency: 2.48003571251426e-5
allele num: 120966
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.549G>A
  hgvsp: ENST00000358139.2:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.237G>A
  hgvsp: ENST00000536095.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.447G>A
  hgvsp: ENST00000346717.4:c.447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.549G>A
  hgvsp: ENST00000435564.1:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.549G>A
  hgvsp: ENST00000331935.6:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.501G>A
  hgvsp: ENST00000409365.1:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.501G>A
  hgvsp: ENST00000351439.5:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.549G>A
  hgvsp: ENST00000456212.1:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.519G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.549G>A
  hgvsp: ENST00000410103.1:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu183Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

2-183095778-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095778
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095778
    reference: chr 2
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.498A>G
  hgvsp: ENST00000409365.1:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.516A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.546A>G
  hgvsp: ENST00000358139.2:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.444A>G
  hgvsp: ENST00000346717.4:c.444A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.498A>G
  hgvsp: ENST00000351439.5:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.546A>G
  hgvsp: ENST00000410103.1:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.234A>G
  hgvsp: ENST00000536095.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.546A>G
  hgvsp: ENST00000456212.1:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.546A>G
  hgvsp: ENST00000435564.1:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.546A>G
  hgvsp: ENST00000331935.6:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8582
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu182Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

2-183095790-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095790
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095790
    reference: chr 2
allele count: 2
allele frequency: 1.65144584083365e-5
allele num: 121106
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.432T>C
  hgvsp: ENST00000346717.4:c.432T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.534T>C
  hgvsp: ENST00000331935.6:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.534T>C
  hgvsp: ENST00000410103.1:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.534T>C
  hgvsp: ENST00000358139.2:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.486T>C
  hgvsp: ENST00000351439.5:c.486T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.504T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.222T>C
  hgvsp: ENST00000536095.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.534T>C
  hgvsp: ENST00000456212.1:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.532T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.486T>C
  hgvsp: ENST00000409365.1:c.486T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.534T>C
  hgvsp: ENST00000435564.1:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe178Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/2-183095791-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095791
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095791
    reference: chr 2
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.533T>G
  hgvsp: ENSP00000410309.1:p.Phe178Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.533T>G
  hgvsp: ENSP00000331574.6:p.Phe178Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.533T>G
  hgvsp: ENSP00000387037.1:p.Phe178Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.485T>G
  hgvsp: ENSP00000309269.9:p.Phe162Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.531T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.485T>G
  hgvsp: ENSP00000386767.1:p.Phe162Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.431T>G
  hgvsp: ENSP00000329112.4:p.Phe144Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.221T>G
  hgvsp: ENSP00000439938.1:p.Phe74Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.533T>G
  hgvsp: ENSP00000408874.1:p.Phe178Cys
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.503T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.533T>G
  hgvsp: ENSP00000350858.2:p.Phe178Cys
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe178Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

2-183095796-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095796
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095796
    reference: chr 2
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.528G>A
  hgvsp: ENST00000331935.6:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.526G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.528G>A
  hgvsp: ENST00000358139.2:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.480G>A
  hgvsp: ENST00000351439.5:c.480G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.528G>A
  hgvsp: ENST00000410103.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.528G>A
  hgvsp: ENST00000456212.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.216G>A
  hgvsp: ENST00000536095.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.528G>A
  hgvsp: ENST00000435564.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.480G>A
  hgvsp: ENST00000409365.1:c.480G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.426G>A
  hgvsp: ENST00000346717.4:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.498G>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu176Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

2-183095811-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095811
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095811
    reference: chr 2
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.513T>C
  hgvsp: ENST00000435564.1:c.513T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.513T>C
  hgvsp: ENST00000456212.1:c.513T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.483T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.465T>C
  hgvsp: ENST00000351439.5:c.465T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.465T>C
  hgvsp: ENST00000409365.1:c.465T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.513T>C
  hgvsp: ENST00000358139.2:c.513T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.411T>C
  hgvsp: ENST00000346717.4:c.411T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.201T>C
  hgvsp: ENST00000536095.1:c.201T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.511T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.513T>C
  hgvsp: ENST00000410103.1:c.513T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.513T>C
  hgvsp: ENST00000331935.6:c.513T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser171Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

2-183095828-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095828
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095828
    reference: chr 2
allele count: 1
allele frequency: 8.257501940512956e-6
allele num: 121102
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.496G>C
  hgvsp: ENSP00000350858.2:p.Ala166Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.496G>C
  hgvsp: ENSP00000410309.1:p.Ala166Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.448G>C
  hgvsp: ENSP00000309269.9:p.Ala150Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.184G>C
  hgvsp: ENSP00000439938.1:p.Ala62Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.448G>C
  hgvsp: ENSP00000386767.1:p.Ala150Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.496G>C
  hgvsp: ENSP00000408874.1:p.Ala166Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.494G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.466G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.496G>C
  hgvsp: ENSP00000387037.1:p.Ala166Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.394G>C
  hgvsp: ENSP00000329112.4:p.Ala132Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.496G>C
  hgvsp: ENSP00000331574.6:p.Ala166Pro
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala166Pro
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

2-183095837-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095837
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095837
    reference: chr 2
allele count: 3
allele frequency: 2.478806206930742e-5
allele num: 121026
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.487G>A
  hgvsp: ENSP00000410309.1:p.Asp163Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.487G>A
  hgvsp: ENSP00000331574.6:p.Asp163Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.175G>A
  hgvsp: ENSP00000439938.1:p.Asp59Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.439G>A
  hgvsp: ENSP00000386767.1:p.Asp147Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.487G>A
  hgvsp: ENSP00000408874.1:p.Asp163Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.487G>A
  hgvsp: ENSP00000350858.2:p.Asp163Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.439G>A
  hgvsp: ENSP00000309269.9:p.Asp147Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.457G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.487G>A
  hgvsp: ENSP00000387037.1:p.Asp163Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.485G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.385G>A
  hgvsp: ENSP00000329112.4:p.Asp129Asn
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp163Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

2-183095838-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095838
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095838
    reference: chr 2
allele count: 8
allele frequency: 6.611788819465106e-5
allele num: 120996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.174C>T
  hgvsp: ENST00000536095.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.438C>T
  hgvsp: ENST00000351439.5:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.384C>T
  hgvsp: ENST00000346717.4:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.486C>T
  hgvsp: ENST00000435564.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.484C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.486C>T
  hgvsp: ENST00000456212.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.486C>T
  hgvsp: ENST00000331935.6:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.486C>T
  hgvsp: ENST00000410103.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.456C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.438C>T
  hgvsp: ENST00000409365.1:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.486C>T
  hgvsp: ENST00000358139.2:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4248
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe162Phe
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

2-183095838-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095838
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095837
    reference: chr 2
allele count: 1
allele frequency: 8.264736024331383e-6
allele num: 120996
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.485delT
  hgvsp: ENSP00000331574.6:p.Phe162SerfsTer6
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.437delT
  hgvsp: ENSP00000309269.9:p.Phe146SerfsTer6
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.485delT
  hgvsp: ENSP00000387037.1:p.Phe162SerfsTer6
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.455delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.173delT
  hgvsp: ENSP00000439938.1:p.Phe58SerfsTer6
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.383delT
  hgvsp: ENSP00000329112.4:p.Phe128SerfsTer6
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.437delT
  hgvsp: ENSP00000386767.1:p.Phe146SerfsTer6
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.485delT
  hgvsp: ENSP00000408874.1:p.Phe162SerfsTer6
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.485delT
  hgvsp: ENSP00000350858.2:p.Phe162SerfsTer6
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.483delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.485delT
  hgvsp: ENSP00000410309.1:p.Phe162SerfsTer6
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe162SerfsTer6
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: GA
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-183095843-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095843
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095843
    reference: chr 2
allele count: 1
allele frequency: 8.274036074797286e-6
allele num: 120860
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.481T>C
  hgvsp: ENSP00000408874.1:p.Ser161Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.433T>C
  hgvsp: ENSP00000386767.1:p.Ser145Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.479T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.433T>C
  hgvsp: ENSP00000309269.9:p.Ser145Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.481T>C
  hgvsp: ENSP00000350858.2:p.Ser161Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.451T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.379T>C
  hgvsp: ENSP00000329112.4:p.Ser127Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.481T>C
  hgvsp: ENSP00000387037.1:p.Ser161Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.481T>C
  hgvsp: ENSP00000410309.1:p.Ser161Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.481T>C
  hgvsp: ENSP00000331574.6:p.Ser161Pro
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.169T>C
  hgvsp: ENSP00000439938.1:p.Ser57Pro
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser161Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-183095858-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095858
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095858
    reference: chr 2
allele count: 1
allele frequency: 8.331805835596807e-6
allele num: 120022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418G>T
  hgvsp: ENSP00000386767.1:p.Asp140Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466G>T
  hgvsp: ENSP00000387037.1:p.Asp156Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466G>T
  hgvsp: ENSP00000350858.2:p.Asp156Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154G>T
  hgvsp: ENSP00000439938.1:p.Asp52Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466G>T
  hgvsp: ENSP00000331574.6:p.Asp156Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466G>T
  hgvsp: ENSP00000408874.1:p.Asp156Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466G>T
  hgvsp: ENSP00000410309.1:p.Asp156Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418G>T
  hgvsp: ENSP00000309269.9:p.Asp140Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364G>T
  hgvsp: ENSP00000329112.4:p.Asp122Tyr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436G>T
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp156Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

2-183095858-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095858
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095858
    reference: chr 2
allele count: 2
allele frequency: 1.666361167119361e-5
allele num: 120022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466G>A
  hgvsp: ENSP00000408874.1:p.Asp156Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364G>A
  hgvsp: ENSP00000329112.4:p.Asp122Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154G>A
  hgvsp: ENSP00000439938.1:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466G>A
  hgvsp: ENSP00000410309.1:p.Asp156Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466G>A
  hgvsp: ENSP00000331574.6:p.Asp156Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466G>A
  hgvsp: ENSP00000350858.2:p.Asp156Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418G>A
  hgvsp: ENSP00000386767.1:p.Asp140Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418G>A
  hgvsp: ENSP00000309269.9:p.Asp140Asn
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466G>A
  hgvsp: ENSP00000387037.1:p.Asp156Asn
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp156Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

2-183095864-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095864
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095864
    reference: chr 2
allele count: 1
allele frequency: 8.360225391676559e-6
allele num: 119614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154-6C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364-6C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466-6C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466-6C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418-6C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436-6C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418-6C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466-6C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464-6C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466-6C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466-6C>G
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.466-6C>G
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

2-183095864-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095864
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095865
    reference: chr 2
allele count: 2
allele frequency: 1.672045078335312e-5
allele num: 119614
alternate allele: GA
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466-7dupT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466-7dupT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364-7dupT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466-7dupT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154-7dupT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466-7dupT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436-7dupT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464-7dupT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466-7dupT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418-7dupT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418-7dupT
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.466-7dupT
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-183095875-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095875
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095875
    reference: chr 2
allele count: 1
allele frequency: 8.397433744247758e-6
allele num: 119084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466-17T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466-17T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154-17T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418-17T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466-17T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364-17T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464-17T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418-17T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466-17T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466-17T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436-17T>C
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

2-183095883-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095883
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095883
    reference: chr 2
allele count: 10
allele frequency: 8.428576244900711e-5
allele num: 118644
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154-25A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418-25A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418-25A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466-25A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436-25A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466-25A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466-25A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466-25A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464-25A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466-25A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364-25A>G
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3634
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

2-183095884-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095884
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095884
    reference: chr 2
allele count: 1
allele frequency: 8.427297702718647e-6
allele num: 118662
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466-26T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464-26T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436-26T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154-26T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466-26T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364-26T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418-26T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418-26T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466-26T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466-26T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466-26T>C
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

2-183095889-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095889
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095889
    reference: chr 2
allele count: 134
allele frequency: 1.132885815255068e-3
allele num: 118282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466-31G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436-31G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418-31G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154-31G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466-31G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466-31G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464-31G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418-31G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466-31G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466-31G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364-31G>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4197
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 7.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2111
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-183095891-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095891
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095891
    reference: chr 2
allele count: 1
allele frequency: 8.454085859695991e-6
allele num: 118286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464-33T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418-33T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466-33T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436-33T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154-33T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466-33T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466-33T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418-33T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466-33T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466-33T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364-33T>C
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5092
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/2-183095909-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095909
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095909
    reference: chr 2
allele count: 32
allele frequency: 2.747724540614803e-4
allele num: 116460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364-51G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418-51G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418-51G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464-51G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436-51G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466-51G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466-51G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466-51G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466-51G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466-51G>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154-51G>T
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS

2-183095909-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095909
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095909
    reference: chr 2
allele count: 1
allele frequency: 8.58663918942126e-6
allele num: 116460
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466-51G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436-51G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418-51G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466-51G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364-51G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464-51G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154-51G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466-51G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466-51G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466-51G>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418-51G>C
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 2.75e1
  variant carriers: 0
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: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

2-183095909-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095909
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095909
    reference: chr 2
allele count: 11
allele frequency: 9.445303108363386e-5
allele num: 116460
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466-51G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466-51G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364-51G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418-51G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436-51G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418-51G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466-51G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466-51G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154-51G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466-51G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464-51G>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

2-183095910-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183095910
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183095910
    reference: chr 2
allele count: 5
allele frequency: 4.298339121763351e-5
allele num: 116324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.466-52C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.466-52C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.418-52C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.466-52C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.154-52C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.466-52C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.464-52C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.418-52C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.466-52C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.436-52C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.364-52C>T
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

2-183099108-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099108
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099108
    reference: chr 2
allele count: 34
allele frequency: 2.833522234815655e-4
allele num: 119992
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.465+51C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.465+51C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.417+51C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.435+51C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.363+51C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.417+51C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.153+51C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.465+51C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.463+51C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.465+51C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.465+51C>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13349
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9078
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

2-183099110-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099110
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099111
    reference: chr 2
allele count: 2
allele frequency: 1.667834150572067e-5
allele num: 119916
alternate allele: AT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.465+48dupA
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.465+48dupA
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.463+48dupA
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.465+48dupA
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.417+48dupA
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.465+48dupA
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.417+48dupA
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.153+48dupA
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.465+48dupA
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.363+48dupA
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.435+48dupA
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4967
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9356
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

2-183099117-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099117
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099117
    reference: chr 2
allele count: 22
allele frequency: 1.832539232999034e-4
allele num: 120052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.363+42T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.465+42T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.417+42T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.465+42T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.153+42T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.435+42T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.417+42T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.465+42T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.465+42T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.463+42T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.465+42T>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13359
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19557
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

2-183099136-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099136
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099136
    reference: chr 2
allele count: 13
allele frequency: 1.077889988889442e-4
allele num: 120606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.465+23G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.465+23G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.153+23G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.417+23G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.463+23G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.417+23G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.363+23G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.465+23G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.465+23G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.435+23G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.465+23G>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

2-183099146-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099146
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099146
    reference: chr 2
allele count: 2
allele frequency: 1.655053706492776e-5
allele num: 120842
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.465+13C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.465+13C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.465+13C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.465+13C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.435+13C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.463+13C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.465+13C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.153+13C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.363+13C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.417+13C>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.417+13C>G
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

2-183099146-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099146
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099146
    reference: chr 2
allele count: 3
allele frequency: 2.482580559739164e-5
allele num: 120842
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.465+13C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.465+13C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.465+13C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.463+13C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.363+13C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.417+13C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.465+13C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.417+13C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.465+13C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.435+13C>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.153+13C>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20763
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ

2-183099158-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099158
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099158
    reference: chr 2
allele count: 1
allele frequency: 8.260093834665961e-6
allele num: 121064
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.465+1G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.465+1G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.465+1G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.465+1G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.417+1G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.363+1G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.463+1G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.465+1G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.435+1G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.417+1G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.153+1G>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9665
  bin: 6.75e1
  variant carriers: 0
hgvs: c.465+1G>A
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-183099162-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099162
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099161
    reference: chr 2
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.413delT
  hgvsp: ENSP00000386767.1:p.Leu138Ter
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.413delT
  hgvsp: ENSP00000309269.9:p.Leu138Ter
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.459delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.461delT
  hgvsp: ENSP00000387037.1:p.Leu154Ter
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.461delT
  hgvsp: ENSP00000410309.1:p.Leu154Ter
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.149delT
  hgvsp: ENSP00000439938.1:p.Leu50Ter
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.561delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.461delT
  hgvsp: ENSP00000350858.2:p.Leu154Ter
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.359delT
  hgvsp: ENSP00000329112.4:p.Leu120Ter
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.461delT
  hgvsp: ENSP00000408874.1:p.Leu154Ter
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.461delT
  hgvsp: ENSP00000331574.6:p.Leu154Ter
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.431delT
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.549delT
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu154Ter
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: TA
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

2-183099166-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099166
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099166
    reference: chr 2
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.410C>T
  hgvsp: ENSP00000386767.1:p.Thr137Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.458C>T
  hgvsp: ENSP00000408874.1:p.Thr153Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.428C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.146C>T
  hgvsp: ENSP00000439938.1:p.Thr49Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.458C>T
  hgvsp: ENSP00000331574.6:p.Thr153Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.458C>T
  hgvsp: ENSP00000387037.1:p.Thr153Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.458C>T
  hgvsp: ENSP00000350858.2:p.Thr153Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.558C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.546C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.410C>T
  hgvsp: ENSP00000309269.9:p.Thr137Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.458C>T
  hgvsp: ENSP00000410309.1:p.Thr153Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.356C>T
  hgvsp: ENSP00000329112.4:p.Thr119Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.456C>T
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr153Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

2-183099170-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099170
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099170
    reference: chr 2
allele count: 18
allele frequency: 1.486080380436577e-4
allele num: 121124
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.454G>A
  hgvsp: ENSP00000410309.1:p.Val152Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.142G>A
  hgvsp: ENSP00000439938.1:p.Val48Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.454G>A
  hgvsp: ENSP00000350858.2:p.Val152Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.454G>A
  hgvsp: ENSP00000331574.6:p.Val152Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.452G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.554G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.424G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.454G>A
  hgvsp: ENSP00000387037.1:p.Val152Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.406G>A
  hgvsp: ENSP00000386767.1:p.Val136Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.406G>A
  hgvsp: ENSP00000309269.9:p.Val136Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.454G>A
  hgvsp: ENSP00000408874.1:p.Val152Ile
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.542G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.352G>A
  hgvsp: ENSP00000329112.4:p.Val118Ile
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val152Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

2-183099171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099171
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099171
    reference: chr 2
allele count: 1
allele frequency: 8.255047961828658e-6
allele num: 121138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.405C>T
  hgvsp: ENST00000351439.5:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.553C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.351C>T
  hgvsp: ENST00000346717.4:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.453C>T
  hgvsp: ENST00000435564.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.453C>T
  hgvsp: ENST00000410103.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.541C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.453C>T
  hgvsp: ENST00000331935.6:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.405C>T
  hgvsp: ENST00000409365.1:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.451C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.423C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.453C>T
  hgvsp: ENST00000358139.2:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.453C>T
  hgvsp: ENST00000456212.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.141C>T
  hgvsp: ENST00000536095.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile151Ile
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

2-183099173-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099173
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099173
    reference: chr 2
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.349A>G
  hgvsp: ENSP00000329112.4:p.Ile117Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.403A>G
  hgvsp: ENSP00000386767.1:p.Ile135Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.139A>G
  hgvsp: ENSP00000439938.1:p.Ile47Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.451A>G
  hgvsp: ENSP00000387037.1:p.Ile151Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.403A>G
  hgvsp: ENSP00000309269.9:p.Ile135Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.421A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.451A>G
  hgvsp: ENSP00000408874.1:p.Ile151Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.451A>G
  hgvsp: ENSP00000331574.6:p.Ile151Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.551A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.451A>G
  hgvsp: ENSP00000350858.2:p.Ile151Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.539A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.449A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.451A>G
  hgvsp: ENSP00000410309.1:p.Ile151Val
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile151Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

2-183099181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099181
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099181
    reference: chr 2
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.131C>T
  hgvsp: ENSP00000439938.1:p.Ala44Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.395C>T
  hgvsp: ENSP00000309269.9:p.Ala132Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.395C>T
  hgvsp: ENSP00000386767.1:p.Ala132Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.441C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.341C>T
  hgvsp: ENSP00000329112.4:p.Ala114Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.413C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.443C>T
  hgvsp: ENSP00000408874.1:p.Ala148Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.443C>T
  hgvsp: ENSP00000331574.6:p.Ala148Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.443C>T
  hgvsp: ENSP00000350858.2:p.Ala148Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.443C>T
  hgvsp: ENSP00000410309.1:p.Ala148Val
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.531C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.543C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.443C>T
  hgvsp: ENSP00000387037.1:p.Ala148Val
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala148Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

2-183099187-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099187
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099187
    reference: chr 2
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.125A>C
  hgvsp: ENSP00000439938.1:p.Tyr42Ser
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.437A>C
  hgvsp: ENSP00000331574.6:p.Tyr146Ser
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.437A>C
  hgvsp: ENSP00000410309.1:p.Tyr146Ser
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.435A>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.437A>C
  hgvsp: ENSP00000387037.1:p.Tyr146Ser
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.407A>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.389A>C
  hgvsp: ENSP00000386767.1:p.Tyr130Ser
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.437A>C
  hgvsp: ENSP00000350858.2:p.Tyr146Ser
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.335A>C
  hgvsp: ENSP00000329112.4:p.Tyr112Ser
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.525A>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.537A>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.437A>C
  hgvsp: ENSP00000408874.1:p.Tyr146Ser
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.389A>C
  hgvsp: ENSP00000309269.9:p.Tyr130Ser
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr146Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

2-183099189-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099189
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099189
    reference: chr 2
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.387A>G
  hgvsp: ENST00000351439.5:c.387A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.333A>G
  hgvsp: ENST00000346717.4:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.435A>G
  hgvsp: ENST00000331935.6:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.435A>G
  hgvsp: ENST00000456212.1:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.435A>G
  hgvsp: ENST00000435564.1:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.523A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.405A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.387A>G
  hgvsp: ENST00000409365.1:c.387A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.435A>G
  hgvsp: ENST00000410103.1:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.435A>G
  hgvsp: ENST00000358139.2:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.433A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.123A>G
  hgvsp: ENST00000536095.1:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.535A>G
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala145Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-183099202-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099202
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099202
    reference: chr 2
allele count: 3
allele frequency: 2.476309967973058e-5
allele num: 121148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.320T>C
  hgvsp: ENSP00000329112.4:p.Met107Thr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.374T>C
  hgvsp: ENSP00000309269.9:p.Met125Thr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.422T>C
  hgvsp: ENSP00000410309.1:p.Met141Thr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.110T>C
  hgvsp: ENSP00000439938.1:p.Met37Thr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.422T>C
  hgvsp: ENSP00000331574.6:p.Met141Thr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.374T>C
  hgvsp: ENSP00000386767.1:p.Met125Thr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.510T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.392T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.422T>C
  hgvsp: ENSP00000408874.1:p.Met141Thr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.422T>C
  hgvsp: ENSP00000387037.1:p.Met141Thr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.422T>C
  hgvsp: ENSP00000350858.2:p.Met141Thr
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.522T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.420T>C
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Met141Thr
num of homozygotes: 1
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

2-183099205-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099205
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099205
    reference: chr 2
allele count: 1
allele frequency: 8.25559316436886e-6
allele num: 121130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.507A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.419A>T
  hgvsp: ENSP00000331574.6:p.His140Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.419A>T
  hgvsp: ENSP00000387037.1:p.His140Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.107A>T
  hgvsp: ENSP00000439938.1:p.His36Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.419A>T
  hgvsp: ENSP00000408874.1:p.His140Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.389A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.417A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.419A>T
  hgvsp: ENSP00000410309.1:p.His140Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.371A>T
  hgvsp: ENSP00000309269.9:p.His124Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.419A>T
  hgvsp: ENSP00000350858.2:p.His140Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.371A>T
  hgvsp: ENSP00000386767.1:p.His124Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.317A>T
  hgvsp: ENSP00000329112.4:p.His106Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.519A>T
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13907
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His140Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

2-183099215-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099215
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099215
    reference: chr 2
allele count: 3
allele frequency: 2.480199738752294e-5
allele num: 120958
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.407A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.409A>G
  hgvsp: ENSP00000350858.2:p.Lys137Glu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.379A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.409A>G
  hgvsp: ENSP00000410309.1:p.Lys137Glu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.361A>G
  hgvsp: ENSP00000309269.9:p.Lys121Glu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.409A>G
  hgvsp: ENSP00000408874.1:p.Lys137Glu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.409A>G
  hgvsp: ENSP00000331574.6:p.Lys137Glu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.497A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.509A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.361A>G
  hgvsp: ENSP00000386767.1:p.Lys121Glu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.409A>G
  hgvsp: ENSP00000387037.1:p.Lys137Glu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.307A>G
  hgvsp: ENSP00000329112.4:p.Lys103Glu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.97A>G
  hgvsp: ENSP00000439938.1:p.Lys33Glu
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys137Glu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

2-183099217-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099217
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099217
    reference: chr 2
allele count: 2
allele frequency: 1.653603201375798e-5
allele num: 120948
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.407G>A
  hgvsp: ENSP00000410309.1:p.Arg136Gln
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.495G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.407G>A
  hgvsp: ENSP00000387037.1:p.Arg136Gln
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.407G>A
  hgvsp: ENSP00000408874.1:p.Arg136Gln
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.359G>A
  hgvsp: ENSP00000309269.9:p.Arg120Gln
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.359G>A
  hgvsp: ENSP00000386767.1:p.Arg120Gln
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.305G>A
  hgvsp: ENSP00000329112.4:p.Arg102Gln
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.407G>A
  hgvsp: ENSP00000331574.6:p.Arg136Gln
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.407G>A
  hgvsp: ENSP00000350858.2:p.Arg136Gln
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.405G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.95G>A
  hgvsp: ENSP00000439938.1:p.Arg32Gln
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.507G>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.377G>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg136Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

2-183099224-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099224
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099224
    reference: chr 2
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.352A>C
  hgvsp: ENSP00000309269.9:p.Met118Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.352A>C
  hgvsp: ENSP00000386767.1:p.Met118Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.298A>C
  hgvsp: ENSP00000329112.4:p.Met100Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.88A>C
  hgvsp: ENSP00000439938.1:p.Met30Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.400A>C
  hgvsp: ENSP00000410309.1:p.Met134Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.398A>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.500A>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.488A>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.400A>C
  hgvsp: ENSP00000350858.2:p.Met134Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.370A>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.400A>C
  hgvsp: ENSP00000331574.6:p.Met134Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.400A>C
  hgvsp: ENSP00000408874.1:p.Met134Leu
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.400A>C
  hgvsp: ENSP00000387037.1:p.Met134Leu
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met134Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum

2-183099227-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099227
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099227
    reference: chr 2
allele count: 1
allele frequency: 8.29462508294625e-6
allele num: 120560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.397-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.87-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.487-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.399-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.399-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.499-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.351-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.297-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.399-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.399-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.399-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.369-2A>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.351-2A>T
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.399-2A>T
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

2-183099234-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099234
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099234
    reference: chr 2
allele count: 1
allele frequency: 8.328058896032513e-6
allele num: 120076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.399-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.499-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.399-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.369-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.397-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.351-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.351-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.399-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.399-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.297-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.399-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.487-9C>T
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.87-9C>T
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20768
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS

2-183099235-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099235
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099235
    reference: chr 2
allele count: 1
allele frequency: 8.333333333333334e-6
allele num: 120000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.397-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.297-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.351-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.487-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.87-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.351-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.399-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.399-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.369-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.399-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.499-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.399-10T>A
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.399-10T>A
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

2-183099241-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099241
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099241
    reference: chr 2
allele count: 10
allele frequency: 8.425309630128907e-5
allele num: 118690
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.399-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.397-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.87-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.369-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.399-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.351-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.297-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.399-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.487-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.399-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.351-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.499-16T>C
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.399-16T>C
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19744
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

2-183099242-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099242
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099242
    reference: chr 2
allele count: 1
allele frequency: 8.426871608184177e-6
allele num: 118668
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.399-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.351-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.397-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.87-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.351-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.399-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.297-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.487-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.399-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.369-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.399-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.399-17A>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.499-17A>G
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/2-183099249-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183099249
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 183099249
    reference: chr 2
allele count: 5
allele frequency: 4.249677024546135e-5
allele num: 117656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000329112
  ensembl transcript: ENST00000346717
  gene symbol: PDE1A
  hgvsc: ENST00000346717.4:c.297-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000408874
  ensembl transcript: ENST00000456212
  gene symbol: PDE1A
  hgvsc: ENST00000456212.1:c.399-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000462938
  gene symbol: PDE1A
  hgvsc: ENST00000462938.1:n.397-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000309269
  ensembl transcript: ENST00000351439
  gene symbol: PDE1A
  hgvsc: ENST00000351439.5:c.351-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000386767
  ensembl transcript: ENST00000409365
  gene symbol: PDE1A
  hgvsc: ENST00000409365.1:c.351-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482782
  gene symbol: PDE1A
  hgvsc: ENST00000482782.1:n.487-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000350858
  ensembl transcript: ENST00000358139
  gene symbol: PDE1A
  hgvsc: ENST00000358139.2:c.399-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000410309
  ensembl transcript: ENST00000435564
  gene symbol: PDE1A
  hgvsc: ENST00000435564.1:c.399-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000387037
  ensembl transcript: ENST00000410103
  gene symbol: PDE1A
  hgvsc: ENST00000410103.1:c.399-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000482538
  gene symbol: PDE1A
  hgvsc: ENST00000482538.1:n.369-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000331574
  ensembl transcript: ENST00000331935
  gene symbol: PDE1A
  hgvsc: ENST00000331935.6:c.399-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl protein: ENSP00000439938
  ensembl transcript: ENST00000536095
  gene symbol: PDE1A
  hgvsc: ENST00000536095.1:c.87-24T>G
  variant of: http://identifiers.org/hgnc/8774
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115252
  ensembl transcript: ENST00000495511
  gene symbol: PDE1A
  hgvsc: ENST00000495511.1:n.499-24T>G
  variant of: http://identifiers.org/hgnc/8774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8432
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 9112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1844
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 9.75e1
variant carriers: 51

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

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

GenotypeQuality
all individuals: 1598
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43617
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.743983257760725e-4
allele num: 11468
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 52
allele frequency: 7.831325301204819e-4
allele num: 66400
num of homozygotes: 2

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.82e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

DP
type: SiteQuality
SIO_000300: 1.83203e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.198e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

FS
type: SiteQuality
SIO_000300: 2.517e0

QD
type: SiteQuality
SIO_000300: 1.327e1

GenotypeQuality
all individuals: 435
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8279
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 387
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1260
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34813
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.066780456582035e-4
allele num: 9374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11078
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.357e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 1.644361e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.48e-1

GenotypeQuality
all individuals: 332
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17573
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2334
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5416
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 9.75e1
variant carriers: 26

GenotypeQuality
all individuals: 1077
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9153
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8342
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.569582652606565e-5
allele num: 53864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5912
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.049245311785333e-4
allele num: 13118
num of homozygotes: 0

East Asian
type: Population
allele count: 18
allele frequency: 2.561183836084235e-3
allele num: 7028
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

DP
type: SiteQuality
SIO_000300: 1.048893e6

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.631e0

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.95e-2

QD
type: SiteQuality
SIO_000300: 1.144e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.26e-1

GenotypeQuality
all individuals: 651
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5416
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1045
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1651
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8342
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17573
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9153
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 181
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 429
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5912
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.271940981938438e-3
allele num: 7862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7028
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13118
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.95e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0

QD
type: SiteQuality
SIO_000300: 1.144e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.631e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.048893e6

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

African
type: Population
allele count: 2
allele frequency: 2.543881963876876e-4
allele num: 7862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7028
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.048893e6

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.26e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.95e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.631e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1857
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6591
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5915
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9808
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6878
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12834
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7688
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.773442511603336e-5
allele num: 53002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5864
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 1.432e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.63e-1

DP
type: SiteQuality
SIO_000300: 9.9719e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.736e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1162
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.701773626290512e-4
allele num: 52886
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12828
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

FS
type: SiteQuality
SIO_000300: 1.132e0

DP
type: SiteQuality
SIO_000300: 9.96451e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.78e-1

QD
type: SiteQuality
SIO_000300: 1.36e1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

GenotypeQuality
all individuals: 1030
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6753
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.940767767728913e-5
allele num: 51526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5758
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.46e-1

DP
type: SiteQuality
SIO_000300: 9.79568e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.232e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e0

GenotypeQuality
all individuals: 1678
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3171
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.844457570387872e-5
allele num: 10158
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65554
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.681e0

FS
type: SiteQuality
SIO_000300: 1.0958e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.25e-1

DP
type: SiteQuality
SIO_000300: 3.325662e6

VQSLOD
type: SiteQuality
SIO_000300: -5.205e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

QD
type: SiteQuality
SIO_000300: 1.476e1

GenotypeQuality
all individuals: 939
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 257
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variant carriers: 0

GenotypeQuality
all individuals: 1150
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variant carriers: 0

GenotypeQuality
all individuals: 1612
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variant carriers: 0

GenotypeQuality
all individuals: 1688
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variant carriers: 0

GenotypeQuality
all individuals: 271
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 71
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42181
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1548
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.846396218983852e-5
allele num: 10156
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12964
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.95e-1

DP
type: SiteQuality
SIO_000300: 3.325811e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.713e0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

FS
type: SiteQuality
SIO_000300: 2.042e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.01e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

GenotypeQuality
all individuals: 166
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1693
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
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GenotypeQuality
all individuals: 42178
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 1782
bin: 8.25e1
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GenotypeQuality
all individuals: 636
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variant carriers: 0

GenotypeQuality
all individuals: 2012
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variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 1604
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 3.201121917014725e-4
allele num: 65602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13152
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

DP
type: SiteQuality
SIO_000300: 3.330828e6

QD
type: SiteQuality
SIO_000300: 1.398e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.82e0

FS
type: SiteQuality
SIO_000300: 4.479e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
all individuals: 805
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 89
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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
all individuals: 42170
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523322060750084e-5
allele num: 65646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.134e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.374e0

DP
type: SiteQuality
SIO_000300: 3.337922e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.97e-1

FS
type: SiteQuality
SIO_000300: 5.998e0

VQSLOD
type: SiteQuality
SIO_000300: 6.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.72e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 212
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GenotypeQuality
all individuals: 42176
bin: 9.75e1
variant carriers: 41

GenotypeQuality
all individuals: 168
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 7284
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GenotypeQuality
all individuals: 900
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 3.75e1
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GenotypeQuality
all individuals: 83
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GenotypeQuality
all individuals: 949
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 58
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 1818
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variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 9.25e1
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GenotypeQuality
all individuals: 1147
bin: 8.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 29
allele frequency: 2.510822510822511e-3
allele num: 11550
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.470615455807496e-4
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.206418144528894e-4
allele num: 66312
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.667440061871617e-5
allele num: 10344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15306
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.37961e6

FS
type: SiteQuality
SIO_000300: 1.133e0

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.34e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.183e0

QD
type: SiteQuality
SIO_000300: 1.139e1

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

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.475006475006475e-5
allele num: 15444
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014499743767522e-5
allele num: 66346
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.379432e6

VQSLOD
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SIO_000300: 4.21e-1

BaseQRankSum
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SIO_000300: 2.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.29e-1

QD
type: SiteQuality
SIO_000300: 1.284e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66420
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.358896095637798e-5
allele num: 15726
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.42e-1

DP
type: SiteQuality
SIO_000300: 3.383711e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e0

QD
type: SiteQuality
SIO_000300: 2.142e1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.217e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.73e-2

GenotypeQuality
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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
all individuals: 38
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15862
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504800312998465e-5
allele num: 66454
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.161e0

QD
type: SiteQuality
SIO_000300: 1.571e1

MQRankSum
type: SiteQuality
SIO_000300: -6.43e-1

DP
type: SiteQuality
SIO_000300: 3.386054e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.56e-1

GenotypeQuality
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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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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
all individuals: 1790
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504392827055001e-5
allele num: 66472
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15942
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.234e0

QD
type: SiteQuality
SIO_000300: 1.355e1

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

BaseQRankSum
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SIO_000300: 2.47e0

ReadPosRankSum
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SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 3.387368e6

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50407604608489e-5
allele num: 66486
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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DP
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MQ
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SIO_000300: 5.975e1

BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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SIO_000300: 1.153e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66570
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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.889060092449923e-4
allele num: 10384
num of homozygotes: 0

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 frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

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

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

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

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

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

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

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42163
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2121
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16374
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 5.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 3.395618e6

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

QD
type: SiteQuality
SIO_000300: 1.43e1

GenotypeDepth
all individuals: 3855
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42164
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1919
bin: 6.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.373e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.395579e6

ReadPosRankSum
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SIO_000300: 1.88e0

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-2

MQ
type: SiteQuality
SIO_000300: 5.928e1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

FS
type: SiteQuality
SIO_000300: 1.007e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.987e0

GenotypeDepth
all individuals: 5087
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.099048548426445e-5
allele num: 16396
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.381e0

BaseQRankSum
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SIO_000300: -2.976e0

MQRankSum
type: SiteQuality
SIO_000300: -9.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.189e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

DP
type: SiteQuality
SIO_000300: 3.395871e6

QD
type: SiteQuality
SIO_000300: 6.44e0

GenotypeDepth
all individuals: 1022
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1794
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8727
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42163
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1915
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.158e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.07e-1

QD
type: SiteQuality
SIO_000300: 1.139e1

DP
type: SiteQuality
SIO_000300: 3.396242e6

FS
type: SiteQuality
SIO_000300: 1.423e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.69e-1

MQ
type: SiteQuality
SIO_000300: 5.879e1

GenotypeDepth
all individuals: 3855
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8651
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 1632
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 1911
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variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.106497313141182e-5
allele num: 16376
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.395422e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.448e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

QD
type: SiteQuality
SIO_000300: 9.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.69e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 960
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42164
bin: 9.75e1
variant carriers: 3

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.503693028283192e-5
allele num: 66612
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.394392e6

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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VQSLOD
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SIO_000300: 1.82e0

MQ
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SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.252e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1889
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variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.459609064175748e-4
allele num: 11562
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: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.504504504504505e-5
allele num: 66600
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16314
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.07e-1

QD
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FS
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.955e1

VQSLOD
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SIO_000300: 5.3e0

DP
type: SiteQuality
SIO_000300: 3.394314e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1622
bin: 7.75e1
variant carriers: 0

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

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

Other
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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African
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MQ
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QD
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BaseQRankSum
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FS
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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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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South Asian
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African
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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BaseQRankSum
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DP
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InbreedingCoeff
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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Other
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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MQ
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DP
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MQRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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QD
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FS
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MQ
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DP
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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African
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allele num: 10172
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.94e0

QD
type: SiteQuality
SIO_000300: 1.563e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 3.33204e6

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

FS
type: SiteQuality
SIO_000300: 2.371e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1765
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42156
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3703
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516300227445034e-5
allele num: 65950
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14910
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

MQRankSum
type: SiteQuality
SIO_000300: 4.55e-1

DP
type: SiteQuality
SIO_000300: 3.33154e6

VQSLOD
type: SiteQuality
SIO_000300: 1.69e-1

FS
type: SiteQuality
SIO_000300: 7.422e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e0

QD
type: SiteQuality
SIO_000300: 1.116e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.22e-1

GenotypeQuality
all individuals: 251
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3332
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2749
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42212
bin: 9.75e1
variant carriers: 131

GenotypeQuality
all individuals: 1759
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 884
bin: 7.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10144
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.605523710265763e-4
allele num: 11514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

South Asian
type: Population
allele count: 83
allele frequency: 5.653180765563275e-3
allele num: 14682
num of homozygotes: 1

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

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 7.137000030370213e-4
allele num: 65854
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.326665e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

FS
type: SiteQuality
SIO_000300: 4.847e0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.014e0

QD
type: SiteQuality
SIO_000300: 1.292e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3197
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1765
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1541
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42140
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518095700752976e-5
allele num: 65872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14686
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

QD
type: SiteQuality
SIO_000300: 1.916e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

DP
type: SiteQuality
SIO_000300: 3.322216e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 1500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1910
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1753
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1525
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42151
bin: 9.75e1
variant carriers: 31

African
type: Population
allele count: 19
allele frequency: 1.920355771174449e-3
allele num: 9894
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.05791694697572e-5
allele num: 65404
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.926115581565472e-4
allele num: 13670
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.009345794392523e-4
allele num: 8560
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.304211e6

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

QD
type: SiteQuality
SIO_000300: 1.354e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

FS
type: SiteQuality
SIO_000300: 2.365e0

GenotypeQuality
all individuals: 1910
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1753
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1525
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42151
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 161
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1500
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65404
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13670
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

FS
type: SiteQuality
SIO_000300: 2.365e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.354e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 3.304211e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

GenotypeQuality
all individuals: 161
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1910
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1525
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42151
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 570
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1753
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.6447923674393e-5
allele num: 65404
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.926115581565472e-4
allele num: 13670
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.010713563776026e-4
allele num: 9894
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

FS
type: SiteQuality
SIO_000300: 2.365e0

QD
type: SiteQuality
SIO_000300: 1.354e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

DP
type: SiteQuality
SIO_000300: 3.304211e6

GenotypeQuality
all individuals: 1214
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 408
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1816
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42139
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 841
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1523
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.338634237605239e-4
allele num: 8552
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.471237310578196e-4
allele num: 13594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529472943623627e-5
allele num: 65382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.5892e1

QD
type: SiteQuality
SIO_000300: 9.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.792e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.794e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.94e-1

DP
type: SiteQuality
SIO_000300: 3.303778e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 1954
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5995
bin: 9.75e1
variant carriers: 33

GenotypeQuality
all individuals: 599
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2608
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26097
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1214
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1806
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3341
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variant carriers: 0

GenotypeQuality
all individuals: 9388
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 24
allele frequency: 2.809646452821353e-3
allele num: 8542
num of homozygotes: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 4.259980525803311e-4
allele num: 16432
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 2.01450443190975e-4
allele num: 9928
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512493193780628e-5
allele num: 66116
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.744e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.289e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-1

DP
type: SiteQuality
SIO_000300: 1.916492e6

GenotypeQuality
all individuals: 1831
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 93
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GenotypeQuality
all individuals: 137
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 9338
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variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.027642374882679e-5
allele num: 66058
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

DP
type: SiteQuality
SIO_000300: 1.917006e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.21e0

QD
type: SiteQuality
SIO_000300: 1.243e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

FS
type: SiteQuality
SIO_000300: 1.232e0

MQ
type: SiteQuality
SIO_000300: 6.032e1

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 425
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GenotypeQuality
all individuals: 1105
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 22

GenotypeQuality
all individuals: 853
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variant carriers: 0

GenotypeQuality
all individuals: 2527
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.679457182966776e-4
allele num: 8548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.569839158302092e-4
allele num: 66152
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.395e1

DP
type: SiteQuality
SIO_000300: 1.927665e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

FS
type: SiteQuality
SIO_000300: 1.923e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-1

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 169
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GenotypeQuality
all individuals: 5961
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variant carriers: 13

GenotypeQuality
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GenotypeQuality
all individuals: 1224
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 33831
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GenotypeQuality
all individuals: 2045
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variant carriers: 0

GenotypeQuality
all individuals: 41
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GenotypeQuality
all individuals: 189
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variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 3227
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GenotypeQuality
all individuals: 9573
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GenotypeQuality
all individuals: 847
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variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.516530178950561e-4
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.505706628120577e-4
allele num: 66414
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.076072426783327e-5
allele num: 16458
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.609e0

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.238e1

DP
type: SiteQuality
SIO_000300: 1.962106e6

GenotypeQuality
all individuals: 109
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
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variant carriers: 0

GenotypeQuality
all individuals: 9630
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 91
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GenotypeQuality
all individuals: 2052
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3230
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variant carriers: 0

GenotypeQuality
all individuals: 5949
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variant carriers: 2

GenotypeQuality
all individuals: 58
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GenotypeQuality
all individuals: 2548
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GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 34497
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 846
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GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.006343384541382e-5
allele num: 66526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.969357e6

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: 3.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.921e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.176e1

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 109
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variant carriers: 0

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

GenotypeQuality
all individuals: 9630
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GenotypeQuality
all individuals: 846
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.509515076812073e-5
allele num: 66526
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.176e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.921e0

VQSLOD
type: SiteQuality
SIO_000300: 3.29e0

MQRankSum
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SIO_000300: -5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

ClippingRankSum
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SIO_000300: -7.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.969357e6

MQ
type: SiteQuality
SIO_000300: 5.931e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 19
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2560
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GenotypeQuality
all individuals: 175
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

FS
type: SiteQuality
SIO_000300: 1.5416e1

QD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
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MQ
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MQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -2.651e0

InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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
all individuals: 13
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GenotypeQuality
all individuals: 5945
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variant carriers: 1

GenotypeQuality
all individuals: 846
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variant carriers: 0

GenotypeQuality
all individuals: 9672
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
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
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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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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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FS
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DP
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MQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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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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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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East Asian
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Other
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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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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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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allele num: 11566
num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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allele num: 66634
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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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QD
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MQRankSum
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DP
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MQ
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BaseQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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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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African
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Latino
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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InbreedingCoeff
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VQSLOD
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MQ
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FS
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ClippingRankSum
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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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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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num of homozygotes: 0

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

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

Other
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Latino
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South Asian
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European (Non-Finnish)
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East Asian
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African
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ReadPosRankSum
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MQRankSum
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QD
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MQ
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FS
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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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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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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South Asian
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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African
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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MQ
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DP
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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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GenotypeDepth
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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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European (Non-Finnish)
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Other
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African
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European (Finnish)
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East Asian
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Latino
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South Asian
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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MQ
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FS
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DP
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BaseQRankSum
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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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African
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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QD
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DP
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SIO_000300: 1.963586e6

MQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

FS
type: SiteQuality
SIO_000300: 1.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.606e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

MQ
type: SiteQuality
SIO_000300: 5.663e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3204
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.514096235956757e-5
allele num: 66046
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9998
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MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.529e0

QD
type: SiteQuality
SIO_000300: 2.68e0

MQ
type: SiteQuality
SIO_000300: 5.547e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 1.952337e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.839e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515059693351918e-5
allele num: 66004
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.397e1

VQSLOD
type: SiteQuality
SIO_000300: -3.677e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 2.126e0

MQRankSum
type: SiteQuality
SIO_000300: 7.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e0

QD
type: SiteQuality
SIO_000300: 1.72e1

DP
type: SiteQuality
SIO_000300: 1.949419e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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variant carriers: 10

GenotypeQuality
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variant carriers: 0

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: 16350
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.745845723281441e-5
allele num: 11434
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65206
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

Other
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allele count: 1
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allele num: 890
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East Asian
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allele count: 8
allele frequency: 9.341429238673517e-4
allele num: 8564
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.54e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 8.77e-1

DP
type: SiteQuality
SIO_000300: 1.903536e6

GenotypeDepth
all individuals: 500
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65196
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Other
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allele frequency: 0.0e0
allele num: 888
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 1
allele frequency: 1.535626535626536e-4
allele num: 6512
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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DP
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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