7-44274053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274053
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274053
    reference: chr 7
allele count: 2
allele frequency: 4.896680050925473e-5
allele num: 40844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+185C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.992C>T
  hgvsp: ENSP00000258682.6:p.Thr331Met
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.949C>T
  hgvsp: ENSP00000326600.4:p.Arg317Ter
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*607C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.337C>T
  hgvsp: ENSP00000388951.1:p.Thr113Met
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.680C>T
  hgvsp: ENSP00000422416.2:p.Thr227Met
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1067C>T
  hgvsp: ENSP00000379098.2:p.Thr356Met
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1067C>T
  hgvsp: ENSP00000397937.2:p.Thr356Met
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.995C>T
  hgvsp: ENSP00000379096.2:p.Thr332Met
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.995C>T
  hgvsp: ENSP00000351542.3:p.Thr332Met
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1318C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1067C>T
  hgvsp: ENSP00000326375.5:p.Thr356Met
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.995C>T
  hgvsp: ENSP00000390292.1:p.Thr332Met
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+185C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6253C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg317Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

7-44274055-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274055
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274055
    reference: chr 7
allele count: 3
allele frequency: 7.232749891508752e-5
allele num: 41478
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.990G>C
  hgvsp: ENSP00000258682.6:p.Gln330His
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.993G>C
  hgvsp: ENSP00000390292.1:p.Gln331His
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6251G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.993G>C
  hgvsp: ENSP00000379096.2:p.Gln331His
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.993G>C
  hgvsp: ENSP00000351542.3:p.Gln331His
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.947G>C
  hgvsp: ENSP00000326600.4:p.Arg316Thr
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1065G>C
  hgvsp: ENSP00000379098.2:p.Gln355His
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.678G>C
  hgvsp: ENSP00000422416.2:p.Gln226His
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*605G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1065G>C
  hgvsp: ENSP00000397937.2:p.Gln355His
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+183G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1065G>C
  hgvsp: ENSP00000326375.5:p.Gln355His
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1316G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+183G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.335G>C
  hgvsp: ENSP00000388951.1:p.Gln112His
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln355His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP

7-44274060-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274060
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274060
    reference: chr 7
allele count: 10
allele frequency: 2.35072872590503e-4
allele num: 42540
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.330C>T
  hgvsp: ENSP00000388951.1:p.Pro111Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.985C>T
  hgvsp: ENSP00000258682.6:p.Pro329Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.673C>T
  hgvsp: ENSP00000422416.2:p.Pro225Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1060C>T
  hgvsp: ENSP00000326375.5:p.Pro354Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1060C>T
  hgvsp: ENSP00000379098.2:p.Pro354Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.988C>T
  hgvsp: ENSP00000390292.1:p.Pro330Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.942C>T
  hgvsp: ENST00000353185.3:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1311C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.988C>T
  hgvsp: ENSP00000351542.3:p.Pro330Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6246C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1060C>T
  hgvsp: ENSP00000397937.2:p.Pro354Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.988C>T
  hgvsp: ENSP00000379096.2:p.Pro330Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*600C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+178C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+178C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10100
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro354Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

7-44274074-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274074
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274074
    reference: chr 7
allele count: 2
allele frequency: 4.378092027494418e-5
allele num: 45682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*600-14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1060-14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.330-14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.988-14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.942-14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1060-14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+164C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.988-14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1311-14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.988-14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.985-14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+164C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1060-14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6232C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.673-14C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

7-44274091-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274091
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274091
    reference: chr 7
allele count: 1
allele frequency: 2.055244985202236e-5
allele num: 48656
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.988-31A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+147A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.942-31A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6215A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1060-31A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+147A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1060-31A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.673-31A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.985-31A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.988-31A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1311-31A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.988-31A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.330-31A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*600-31A>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1060-31A>C
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12088
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

7-44274099-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274099
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274099
    reference: chr 7
allele count: 2
allele frequency: 3.901982206961137e-5
allele num: 51256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.985-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.330-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1060-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+139C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.988-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.988-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.942-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6207C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+139C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1060-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1060-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*600-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.988-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.673-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1311-39C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12474
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

7-44274109-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274109
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274109
    reference: chr 7
allele count: 1
allele frequency: 1.787565693039219e-5
allele num: 55942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*600-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.985-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.673-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1060-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.330-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.988-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+129G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1060-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+129G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6197G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.988-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1060-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.942-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.988-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1311-49G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12846
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

7-44274110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274110
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274110
    reference: chr 7
allele count: 16
allele frequency: 2.815909890883492e-4
allele num: 56820
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+128C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1060-50C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.673-50C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+128C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1060-50C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*600-50C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.985-50C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1311-50C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1060-50C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.330-50C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.988-50C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.988-50C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6196C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.988-50C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.942-50C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28256
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS

7-44274191-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274191
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274191
    reference: chr 7
allele count: 4
allele frequency: 3.345264777707156e-5
allele num: 119572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6115C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+47C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+47C>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

7-44274192-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274192
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274192
    reference: chr 7
allele count: 1
allele frequency: 8.362882183715796e-6
allele num: 119576
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6114G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+46G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+46G>C
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

7-44274193-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274193
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274193
    reference: chr 7
allele count: 1
allele frequency: 8.361343835181191e-6
allele num: 119598
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6113T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+45T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+45T>C
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25243
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

7-44274197-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274197
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274197
    reference: chr 7
allele count: 6
allele frequency: 5.015632053232575e-5
allele num: 119626
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6109A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+41A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+41A>G
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25359
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11454
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

7-44274205-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274205
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274205
    reference: chr 7
allele count: 2
allele frequency: 1.67238063383226e-5
allele num: 119590
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6101G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+33G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+33G>C
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-44274205-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274205
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274205
    reference: chr 7
allele count: 1
allele frequency: 8.361903169161301e-6
allele num: 119590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6101G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+33G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+33G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25705
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-44274206-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274206
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274206
    reference: chr 7
allele count: 6
allele frequency: 5.016470745614768e-5
allele num: 119606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+32G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6100G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-44274208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274208
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274208
    reference: chr 7
allele count: 23
allele frequency: 1.922851840085609e-4
allele num: 119614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6098G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+30G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25899
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

7-44274209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274209
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274209
    reference: chr 7
allele count: 15
allele frequency: 1.253467927933951e-4
allele num: 119668
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6097C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+29C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11780
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12207
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

7-44274210-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274210
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274210
    reference: chr 7
allele count: 1
allele frequency: 8.353800143685363e-6
allele num: 119706
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6096C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+28C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+28C>G
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-44274223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274223
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274223
    reference: chr 7
allele count: 44
allele frequency: 3.67064319679653e-4
allele num: 119870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6083G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+15G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+15G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26540
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 3.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
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: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

7-44274224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274224
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274224
    reference: chr 7
allele count: 34
allele frequency: 2.835743715491501e-4
allele num: 119898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6082C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+14C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+14C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11853
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26577
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

7-44274226-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274226
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274226
    reference: chr 7
allele count: 1
allele frequency: 8.337224037884346e-6
allele num: 119944
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6080G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+12G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+12G>C
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-44274232-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274232
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274232
    reference: chr 7
allele count: 2
allele frequency: 1.666194578202842e-5
allele num: 120034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1310+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.987+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.941+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1059+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.984+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.672+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6074G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1059+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.987+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1059+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.987+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.329+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1059+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.987+6G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*599+6G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1059+6G>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

7-44274247-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274247
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274247
    reference: chr 7
allele count: 1
allele frequency: 8.321405984755183e-6
allele num: 120172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.975T>C
  hgvsp: ENST00000258682.6:c.975T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1050T>C
  hgvsp: ENST00000350811.3:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1050T>C
  hgvsp: ENST00000395749.2:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.978T>C
  hgvsp: ENST00000395747.2:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.978T>C
  hgvsp: ENST00000457475.1:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.320T>C
  hgvsp: ENST00000433930.1:c.320T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.978T>C
  hgvsp: ENST00000353625.4:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.932T>C
  hgvsp: ENSP00000326600.4:p.Met311Thr
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6059T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1301T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1050T>C
  hgvsp: ENST00000440254.2:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1050T>C
  hgvsp: ENST00000347193.4:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.663T>C
  hgvsp: ENST00000502837.2:c.663T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*590T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.978T>C
  hgvsp: ENST00000358707.3:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met311Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

7-44274253-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274253
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274253
    reference: chr 7
allele count: 1
allele frequency: 8.320713584396998e-6
allele num: 120182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.972A>G
  hgvsp: ENST00000457475.1:c.972A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1044A>G
  hgvsp: ENST00000350811.3:c.1044A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1044A>G
  hgvsp: ENST00000395749.2:c.1044A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.969A>G
  hgvsp: ENST00000258682.6:c.969A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.657A>G
  hgvsp: ENST00000502837.2:c.657A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1044A>G
  hgvsp: ENST00000440254.2:c.1044A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.926A>G
  hgvsp: ENSP00000326600.4:p.Lys309Arg
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.314A>G
  hgvsp: ENST00000433930.1:c.314A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.972A>G
  hgvsp: ENST00000395747.2:c.972A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*584A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.972A>G
  hgvsp: ENST00000358707.3:c.972A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1044A>G
  hgvsp: ENST00000347193.4:c.1044A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.972A>G
  hgvsp: ENST00000353625.4:c.972A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1295A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6053A>G
  variant of: http://identifiers.org/hgnc/1461
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11811
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys309Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

7-44274284-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274284
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274284
    reference: chr 7
allele count: 3
allele frequency: 2.510166173000653e-5
allele num: 119514
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.947-6A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.947-6A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.635-9A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1022-9A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.947-9A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6022A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.947-6A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1273-9A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.947-6A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.292-9A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1022-9A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1022-9A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.904-9A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*562-9A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1022-9A>G
  variant of: http://identifiers.org/hgnc/1461
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26137
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.947-6A>G
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP

7-44274285-GGGGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274285
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274281
    reference: chr 7
allele count: 1
allele frequency: 8.370862701109976e-6
allele num: 119462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1022-14_1022-11delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1022-14_1022-11delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.635-14_635-11delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.947-11_947-8delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*562-14_*562-11delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1273-14_1273-11delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.292-14_292-11delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.947-14_947-11delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6017_946+6020delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.947-11_947-8delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.947-11_947-8delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.904-14_904-11delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1022-14_1022-11delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.947-11_947-8delTCCC
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1022-14_1022-11delTCCC
  variant of: http://identifiers.org/hgnc/1461
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26055
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.947-11_947-8delTCCC
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: GGGGA
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD

7-44274289-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274289
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274289
    reference: chr 7
allele count: 1
allele frequency: 8.381105635455429e-6
allele num: 119316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.904-14T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6017T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.292-14T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1022-14T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1022-14T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.947-11T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*562-14T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1273-14T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.947-14T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1022-14T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.947-11T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.635-14T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.947-11T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.947-11T>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1022-14T>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11458
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

7-44274298-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274298
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274298
    reference: chr 7
allele count: 5
allele frequency: 4.210384492311838e-5
allele num: 118754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1022-23C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.947-23C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.947-20C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6008C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.947-20C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.947-20C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.635-23C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1022-23C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.947-20C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.904-23C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1022-23C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.292-23C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1022-23C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*562-23C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1273-23C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

7-44274306-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274306
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274306
    reference: chr 7
allele count: 1
allele frequency: 8.443236123541432e-6
allele num: 118438
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.947-28T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*562-31T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1022-31T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1022-31T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.292-31T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.947-28T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+6000T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1022-31T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.947-31T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1022-31T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.947-28T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1273-31T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.947-28T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.635-31T>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.904-31T>C
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

7-44274314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274314
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274314
    reference: chr 7
allele count: 1
allele frequency: 8.483203257550051e-6
allele num: 117880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.947-36C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1022-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1022-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1022-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.635-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*562-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.904-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1273-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+5992C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.947-36C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.292-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.947-36C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.947-36C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.947-39C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1022-39C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9285
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

7-44274315-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274315
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274315
    reference: chr 7
allele count: 2
allele frequency: 1.698254194687861e-5
allele num: 117768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.947-37G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1022-40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1022-40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.947-37G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.292-40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.947-40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1022-40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.947-37G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1273-40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*562-40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.947-37G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1022-40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.635-40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.904-40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+5991G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9163
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-44274324-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44274324
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44274324
    reference: chr 7
allele count: 336
allele frequency: 2.911965056419323e-3
allele num: 115386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.947-46G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1022-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.947-46G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1022-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+5982G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.904-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*562-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.947-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1022-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1273-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.635-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.947-46G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.947-46G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1022-49G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.292-49G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9108
  bin: 2.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9020
  bin: 1.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
num of homozygotes: 9
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

7-44279148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279148
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279148
    reference: chr 7
allele count: 19
allele frequency: 1.058142125194921e-3
allele num: 17956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1158G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1021+40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1158G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1021+40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.634+40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1158G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2151G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1021+40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.291+40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1272+40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1021+40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1158G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1158G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*561+40G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1158G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

7-44279152-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279152
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279152
    reference: chr 7
allele count: 1
allele frequency: 5.462689828471539e-5
allele num: 18306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1154G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1021+36G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.634+36G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.291+36G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1154G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1021+36G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2147G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1154G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*561+36G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1154G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1154G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1154G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1021+36G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1272+36G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1021+36G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

7-44279153-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279153
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279153
    reference: chr 7
allele count: 20
allele frequency: 1.077354018530489e-3
allele num: 18564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.291+35C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1153C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1153C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.634+35C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1021+35C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1021+35C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1021+35C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1153C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1153C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*561+35C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2146C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1272+35C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1021+35C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1153C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1153C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8540
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

7-44279155-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279155
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279155
    reference: chr 7
allele count: 1
allele frequency: 5.368839256952647e-5
allele num: 18626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1151C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1151C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1272+33C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1151C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1021+33C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1151C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1021+33C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2144C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1021+33C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1151C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*561+33C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1021+33C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1151C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.634+33C>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.291+33C>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

7-44279163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279163
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279163
    reference: chr 7
allele count: 1
allele frequency: 5.271481286241434e-5
allele num: 18970
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2136C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1021+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1143C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1021+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1143C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1272+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1143C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1021+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1143C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1143C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1021+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1143C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.634+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.291+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*561+25C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9056
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

7-44279174-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279174
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279174
    reference: chr 7
allele count: 2
allele frequency: 1.027010372804765e-4
allele num: 19474
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1021+14G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1272+14G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1132G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1132G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1021+14G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1132G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1132G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2125G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1132G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1021+14G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.291+14G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1021+14G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.634+14G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1132G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*561+14G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

7-44279175-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279175
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279175
    reference: chr 7
allele count: 1
allele frequency: 5.129257283545343e-5
allele num: 19496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1131C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.1021+13C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1131C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*561+13C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.1021+13C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1131C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1131C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.1021+13C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2124C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.634+13C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1131C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1131C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.1021+13C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.291+13C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1272+13C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10713
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

7-44279215-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279215
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279215
    reference: chr 7
allele count: 2
allele frequency: 9.801038910124473e-5
allele num: 20406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.994G>A
  hgvsp: ENSP00000397937.2:p.Gly332Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1091G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1091G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.264G>A
  hgvsp: ENSP00000388951.1:p.Gly89Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.994G>A
  hgvsp: ENSP00000326375.5:p.Gly332Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.994G>A
  hgvsp: ENSP00000379098.2:p.Gly332Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*534G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2084G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1091G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1245G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.607G>A
  hgvsp: ENSP00000422416.2:p.Gly203Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1091G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1091G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.994G>A
  hgvsp: ENSP00000326544.6:p.Gly332Ser
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1091G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13372
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly332Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

7-44279222-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279222
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279222
    reference: chr 7
allele count: 1
allele frequency: 4.882335709403378e-5
allele num: 20482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1084G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.987G>A
  hgvsp: ENST00000347193.4:c.987G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*527G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1084G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1084G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1238G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.987G>A
  hgvsp: ENST00000395749.2:c.987G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.600G>A
  hgvsp: ENST00000502837.2:c.600G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.987G>A
  hgvsp: ENST00000350811.3:c.987G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.987G>A
  hgvsp: ENST00000440254.2:c.987G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.257G>A
  hgvsp: ENST00000433930.1:c.257G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2077G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1084G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1084G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1084G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala329Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

7-44279233-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279233
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279233
    reference: chr 7
allele count: 2
allele frequency: 9.734254842791784e-5
allele num: 20546
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1227A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.976A>G
  hgvsp: ENSP00000379098.2:p.Met326Val
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1073A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1073A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2066A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.976A>G
  hgvsp: ENSP00000397937.2:p.Met326Val
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.976A>G
  hgvsp: ENSP00000326375.5:p.Met326Val
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1073A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.976A>G
  hgvsp: ENSP00000326544.6:p.Met326Val
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1073A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.589A>G
  hgvsp: ENSP00000422416.2:p.Met197Val
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1073A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.246A>G
  hgvsp: ENSP00000388951.1:p.Met83Val
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*516A>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1073A>G
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met326Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

7-44279240-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279240
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279240
    reference: chr 7
allele count: 1
allele frequency: 4.865233044662839e-5
allele num: 20554
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.239G>A
  hgvsp: ENST00000433930.1:c.239G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1066G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1066G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*509G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.969G>A
  hgvsp: ENST00000440254.2:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.969G>A
  hgvsp: ENST00000350811.3:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.969G>A
  hgvsp: ENST00000347193.4:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.582G>A
  hgvsp: ENST00000502837.2:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1066G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.969G>A
  hgvsp: ENST00000395749.2:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2059G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1066G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1066G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1220G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1066G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12811
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro323Pro
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

7-44279241-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279241
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279241
    reference: chr 7
allele count: 1
allele frequency: 4.865706500583885e-5
allele num: 20552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1065C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.968C>T
  hgvsp: ENSP00000326375.5:p.Pro323Leu
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*508C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.968C>T
  hgvsp: ENSP00000379098.2:p.Pro323Leu
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1065C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1065C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.968C>T
  hgvsp: ENSP00000326544.6:p.Pro323Leu
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1065C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.238C>T
  hgvsp: ENSP00000388951.1:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2058C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.581C>T
  hgvsp: ENSP00000422416.2:p.Pro194Leu
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.968C>T
  hgvsp: ENSP00000397937.2:p.Pro323Leu
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1219C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1065C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1065C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12807
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro323Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

7-44279274-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279274
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279274
    reference: chr 7
allele count: 1
allele frequency: 4.88328938372888e-5
allele num: 20478
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.217-12C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.947-12C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.947-12C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1032C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1032C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.560-12C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1032C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.947-12C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*487-12C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1032C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1032C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.947-12C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2025C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1198-12C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1032C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-44279284-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279284
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279284
    reference: chr 7
allele count: 1
allele frequency: 4.894283476898982e-5
allele num: 20432
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1022G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1022G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.560-22G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.947-22G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1022G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2015G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*487-22G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1022G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.947-22G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1022G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.947-22G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1198-22G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.947-22G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1022G>C
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.217-22G>C
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum

7-44279284-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279284
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279284
    reference: chr 7
allele count: 22
allele frequency: 1.076742364917776e-3
allele num: 20432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1022G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1022G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*487-22G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1022G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.947-22G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1022G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.947-22G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.560-22G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.947-22G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1022G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.947-22G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.217-22G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1198-22G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1022G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+2015G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13181
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

7-44279305-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279305
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279305
    reference: chr 7
allele count: 11
allele frequency: 5.47209232912148e-4
allele num: 20102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.947-43G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1001G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1001G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1001G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1001G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1198-43G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.560-43G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.947-43G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1001G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.947-43G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+1994G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.947-43G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*487-43G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.217-43G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1001G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13595
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

7-44279306-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44279306
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44279306
    reference: chr 7
allele count: 1
allele frequency: 4.95884161459883e-5
allele num: 20166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+1000C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1198-44C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.947-44C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+1000C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.947-44C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+1000C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.947-44C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+1000C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+1000C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+1000C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.560-44C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.217-44C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*487-44C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.947-44C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+1993C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13685
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

7-44280268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280268
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280268
    reference: chr 7
allele count: 2
allele frequency: 1.793046565419304e-5
allele num: 111542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.946+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.946+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.946+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.946+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.559+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1197+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*486+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.216+38C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+1031C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9848
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

7-44280276-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280276
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280276
    reference: chr 7
allele count: 2
allele frequency: 1.785714285714286e-5
allele num: 112000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1197+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.946+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.946+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.946+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+1023G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.559+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.946+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*486+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+30G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.216+30G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

7-44280277-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280277
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280277
    reference: chr 7
allele count: 1
allele frequency: 8.910591128615473e-6
allele num: 112226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.946+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.216+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.559+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.946+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.946+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+1022C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.946+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1197+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*486+29C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+29C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11794
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/7-44280278-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280278
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280278
    reference: chr 7
allele count: 1
allele frequency: 8.889521032606763e-6
allele num: 112492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.946+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.946+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1197+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.216+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.946+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+1021G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.946+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.559+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+28G>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*486+28G>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22375
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-44280279-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280279
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280279
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 112728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.946+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1197+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.946+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.946+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.946+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.216+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*486+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+1020G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.559+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+27G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+27G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-44280281-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280281
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280281
    reference: chr 7
allele count: 2
allele frequency: 1.769692250517635e-5
allele num: 113014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1197+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.946+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.216+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.559+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+1018C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.946+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.946+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*486+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+25C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.946+25C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6077
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

7-44280282-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280282
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280282
    reference: chr 7
allele count: 1
allele frequency: 8.836107871204892e-6
allele num: 113172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.946+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.946+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*486+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.946+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.946+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1197+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+1017A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.216+24A>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.559+24A>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25184
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

7-44280283-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280283
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280283
    reference: chr 7
allele count: 1
allele frequency: 8.823633219214344e-6
allele num: 113332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.216+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.946+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.559+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+1016G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.946+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.946+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.946+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1197+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+23G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*486+23G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25748
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD

7-44280299-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280299
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280299
    reference: chr 7
allele count: 1
allele frequency: 8.637816360024186e-6
allele num: 115770
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.946+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.946+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.946+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.559+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*486+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.946+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1197+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.216+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+1000C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+7C>G
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+7C>G
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30004
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.946+7C>G
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

7-44280303-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280303
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280303
    reference: chr 7
allele count: 1
allele frequency: 8.607481623026734e-6
allele num: 116178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.216+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+996G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.559+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.946+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*486+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.946+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.946+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.946+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.946+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.946+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.946+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.946+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.946+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1197+3G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.946+3G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.946+3G>A
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

7-44280318-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280318
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280318
    reference: chr 7
allele count: 1
allele frequency: 8.571477551300294e-6
allele num: 116666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.934C>T
  hgvsp: ENSP00000326544.6:p.Arg312Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.934C>T
  hgvsp: ENSP00000326427.5:p.Arg312Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.934C>T
  hgvsp: ENSP00000390292.1:p.Arg312Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.934C>T
  hgvsp: ENSP00000326375.5:p.Arg312Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.547C>T
  hgvsp: ENSP00000422416.2:p.Arg183Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*474C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.934C>T
  hgvsp: ENSP00000258682.6:p.Arg312Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.934C>T
  hgvsp: ENSP00000326518.5:p.Arg312Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1185C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.934C>T
  hgvsp: ENSP00000379096.2:p.Arg312Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.934C>T
  hgvsp: ENSP00000379098.2:p.Arg312Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.204C>T
  hgvsp: ENSP00000388951.1:p.Arg69Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.934C>T
  hgvsp: ENSP00000397937.2:p.Arg312Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.934C>T
  hgvsp: ENSP00000351542.3:p.Arg312Trp
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+981C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg312Trp
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

7-44280322-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280322
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280322
    reference: chr 7
allele count: 1
allele frequency: 8.577947811765514e-6
allele num: 116578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.930C>T
  hgvsp: ENST00000353625.4:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.930C>T
  hgvsp: ENST00000258682.6:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.543C>T
  hgvsp: ENST00000502837.2:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+977C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.930C>T
  hgvsp: ENST00000457475.1:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.930C>T
  hgvsp: ENST00000347193.4:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.200C>T
  hgvsp: ENST00000433930.1:c.200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.930C>T
  hgvsp: ENST00000395749.2:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*470C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1181C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.930C>T
  hgvsp: ENST00000346990.4:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.930C>T
  hgvsp: ENST00000440254.2:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.930C>T
  hgvsp: ENST00000358707.3:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.930C>T
  hgvsp: ENST00000395747.2:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.930C>T
  hgvsp: ENST00000350811.3:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14768
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala310Ala
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

7-44280340-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280340
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280340
    reference: chr 7
allele count: 1
allele frequency: 8.647227698799765e-6
allele num: 115644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.912C>T
  hgvsp: ENST00000457475.1:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.182C>T
  hgvsp: ENST00000433930.1:c.182C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.912C>T
  hgvsp: ENST00000395749.2:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.912C>T
  hgvsp: ENST00000347193.4:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.912C>T
  hgvsp: ENST00000346990.4:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1163C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+959C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.912C>T
  hgvsp: ENST00000353625.4:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.912C>T
  hgvsp: ENST00000258682.6:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.912C>T
  hgvsp: ENST00000358707.3:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*452C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.912C>T
  hgvsp: ENST00000395747.2:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.912C>T
  hgvsp: ENST00000440254.2:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.912C>T
  hgvsp: ENST00000350811.3:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.525C>T
  hgvsp: ENST00000502837.2:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile304Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

7-44280356-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280356
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280356
    reference: chr 7
allele count: 2
allele frequency: 1.775505131209829e-5
allele num: 112644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*444-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.904-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.517-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.904-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1155-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.904-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.904-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.904-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.904-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.904-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.904-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+943C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.904-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.904-8C>T
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.174-8C>T
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.904-8C>T
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

7-44280360-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280360
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280360
    reference: chr 7
allele count: 1
allele frequency: 8.947264821144176e-6
allele num: 111766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000258682
  ensembl transcript: ENST00000258682
  gene symbol: CAMK2B
  hgvsc: ENST00000258682.6:c.904-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000390292
  ensembl transcript: ENST00000457475
  gene symbol: CAMK2B
  hgvsc: ENST00000457475.1:c.904-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379096
  ensembl transcript: ENST00000395747
  gene symbol: CAMK2B
  hgvsc: ENST00000395747.2:c.904-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000351542
  ensembl transcript: ENST00000358707
  gene symbol: CAMK2B
  hgvsc: ENST00000358707.3:c.904-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326375
  ensembl transcript: ENST00000350811
  gene symbol: CAMK2B
  hgvsc: ENST00000350811.3:c.904-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326600
  ensembl transcript: ENST00000353185
  gene symbol: CAMK2B
  hgvsc: ENST00000353185.3:c.903+939G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.904-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000388951
  ensembl transcript: ENST00000433930
  gene symbol: CAMK2B
  hgvsc: ENST00000433930.1:c.174-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.904-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000422416
  ensembl transcript: ENST00000502837
  gene symbol: CAMK2B
  hgvsc: ENST00000502837.2:c.517-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000397937
  ensembl transcript: ENST00000440254
  gene symbol: CAMK2B
  hgvsc: ENST00000440254.2:c.904-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl transcript: ENST00000497584
  gene symbol: CAMK2B
  hgvsc: ENST00000497584.1:n.1155-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000379098
  ensembl transcript: ENST00000395749
  gene symbol: CAMK2B
  hgvsc: ENST00000395749.2:c.904-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000428912
  ensembl transcript: ENST00000523845
  gene symbol: CAMK2B
  hgvsc: ENST00000523845.1:c.*444-12G>A
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326518
  ensembl transcript: ENST00000346990
  gene symbol: CAMK2B
  hgvsc: ENST00000346990.4:c.904-12G>A
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9072
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

7-44280362-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44280362
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 44280360
    reference: chr 7
allele count: 1
allele frequency: 9.007061536244416e-6
allele num: 111024
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326544
  ensembl transcript: ENST00000347193
  gene symbol: CAMK2B
  hgvsc: ENST00000347193.4:c.904-16_904-15delCT
  variant of: http://identifiers.org/hgnc/1461
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000058404
  ensembl protein: ENSP00000326427
  ensembl transcript: ENST00000353625
  gene symbol: CAMK2B
  hgvsc: ENST00000353625.4:c.904-16_904-15delCT
  variant of: http://identifiers.org/hgnc/1461
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: CAG

GenotypeDepth
all individuals: 293
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2426
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9514
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 216
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 374
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2380
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34252
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5541
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2675
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1472
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2931
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4547
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2934
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.119634176485128e-5
allele num: 24274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3176
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.604902667627974e-4
allele num: 2774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.226e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.36e-2

QD
type: SiteQuality
SIO_000300: 1.242e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.872e0

VQSLOD
type: SiteQuality
SIO_000300: 9.45e-1

DP
type: SiteQuality
SIO_000300: 9.13082e5

FS
type: SiteQuality
SIO_000300: 1.145e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.61e-1

GenotypeDepth
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 374
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5245
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 388
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34085
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 345
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 342
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4549
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1866
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2955
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 201
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34844
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5396
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2708
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3395
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3210
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1394
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 6.759801712483101e-4
allele num: 4438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

QD
type: SiteQuality
SIO_000300: 9.050000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.16889e5

GenotypeDepth
all individuals: 215
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2684
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 33592
bin: 7.5e0
variant carriers: 3

GenotypeDepth
all individuals: 3485
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 293
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5205
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 209
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 346
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 513
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1342
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2951
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5361
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33844
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2931
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2367
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1525
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 260
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4555
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 125
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 94
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4668
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3266
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.417634996582365e-4
allele num: 2926
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 3.562099263832819e-4
allele num: 25266
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.23e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

FS
type: SiteQuality
SIO_000300: 5.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.056e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

DP
type: SiteQuality
SIO_000300: 9.18595e5

GenotypeDepth
all individuals: 246
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11277
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 332
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 346
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1342
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3502
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2800
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5283
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3414
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32527
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4548
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2317
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1813
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.7821482602118e-4
allele num: 5288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27006
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1610
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

FS
type: SiteQuality
SIO_000300: 3.862e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.69e-1

QD
type: SiteQuality
SIO_000300: 1.009e1

VQSLOD
type: SiteQuality
SIO_000300: 5.53e-1

DP
type: SiteQuality
SIO_000300: 9.28214e5

GenotypeDepth
all individuals: 376
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4084
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 247
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31019
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 345
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1342
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3889
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4547
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2915
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4817
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30675
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3742
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2547
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5082
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5722
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.49283967865875e-5
allele num: 28630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1850
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.45108e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

FS
type: SiteQuality
SIO_000300: 5.756e0

QD
type: SiteQuality
SIO_000300: 4.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.237e0

VQSLOD
type: SiteQuality
SIO_000300: -2.181e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.31e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

GenotypeDepth
all individuals: 3755
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 637
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1342
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 249
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 346
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4232
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4426
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2810
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3911
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29569
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4545
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2907
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2042
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5314
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3790
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.668444918644971e-5
allele num: 29992
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.166e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.372e-1

DP
type: SiteQuality
SIO_000300: 9.60039e5

QD
type: SiteQuality
SIO_000300: 5.51e0

GenotypeDepth
all individuals: 28627
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 967
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 333
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 345
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4398
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1935
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4546
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 524
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2483
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3953
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3449
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4515
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4815
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29305
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2314
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.449779519843214e-4
allele num: 4082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5678
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6828
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.09e-2

DP
type: SiteQuality
SIO_000300: 1.00144e6

VQSLOD
type: SiteQuality
SIO_000300: 4.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-2

FS
type: SiteQuality
SIO_000300: 4.957e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

QD
type: SiteQuality
SIO_000300: 1.465e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.58e-1

GenotypeDepth
all individuals: 12868
bin: 1.25e1
variant carriers: 10

GenotypeDepth
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 346
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1342
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 345
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4535
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4561
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 3925
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3284
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 28835
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 131
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4904
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2514
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 7.25e1
variant carriers: 1

South Asian
type: Population
allele count: 16
allele frequency: 2.294235732721537e-3
allele num: 6974
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4176
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32966
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.09e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 1.00982e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

QD
type: SiteQuality
SIO_000300: 1.119e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 819
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1241
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2928
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1583
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2762
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1194
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2595
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1201
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8995
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4793
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 31717
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.643603436266543e-4
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16370
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: 6278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65730
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.053e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 1.800907e6

FS
type: SiteQuality
SIO_000300: 5.209e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.278e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

GenotypeDepth
all individuals: 660
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2751
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25182
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 819
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 336
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 467
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32285
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2572
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8985
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4785
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2741
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521329033043267e-5
allele num: 65732
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.04e0

FS
type: SiteQuality
SIO_000300: 7.097e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.622e1

MQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

DP
type: SiteQuality
SIO_000300: 1.801894e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1548
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11636
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 336
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 819
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9006
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2740
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 555
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1566
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4785
bin: 9.75e1
variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6278
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521329033043267e-5
allele num: 65732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

VQSLOD
type: SiteQuality
SIO_000300: 9.6e-2

DP
type: SiteQuality
SIO_000300: 1.802904e6

FS
type: SiteQuality
SIO_000300: 2.148e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

QD
type: SiteQuality
SIO_000300: 1.68e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.911e1

GenotypeDepth
all individuals: 11645
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 468
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 659
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1238
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1551
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2558
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9038
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33593
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4780
bin: 9.75e1
variant carriers: 6

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6278
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 6
allele frequency: 3.659875564230816e-4
allele num: 16394
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

DP
type: SiteQuality
SIO_000300: 1.805997e6

QD
type: SiteQuality
SIO_000300: 1.341e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeDepth
all individuals: 98
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1253
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11715
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25705
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 207
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 467
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8995
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4774
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34906
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 602
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2519
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.042658066086533e-5
allele num: 65732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6264
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -6.6e-1

FS
type: SiteQuality
SIO_000300: 2.092e0

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.191e1

DP
type: SiteQuality
SIO_000300: 1.815628e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 8.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.49e-1

GenotypeDepth
all individuals: 467
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 819
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 664
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2863
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8995
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34906
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4774
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 590
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 294
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2519
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65732
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 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: 6264
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.100536847242558e-5
allele num: 16392
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.092e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 8.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.49e-1

QD
type: SiteQuality
SIO_000300: 1.191e1

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

DP
type: SiteQuality
SIO_000300: 1.815628e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.6e-1

GenotypeDepth
all individuals: 25769
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11714
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2850
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 660
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4771
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 34981
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9003
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2671
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1515
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65734
num of homozygotes: 0

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

Latino
type: Population
allele count: 6
allele frequency: 5.221023320570832e-4
allele num: 11492
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
SIO_000300: -2.054e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.24e-1

FS
type: SiteQuality
SIO_000300: 5.757e0

QD
type: SiteQuality
SIO_000300: 1.808e1

DP
type: SiteQuality
SIO_000300: 1.816341e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.68e-1

GenotypeDepth
all individuals: 12195
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11795
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 664
bin: 4.75e1
variant carriers: 3

GenotypeDepth
all individuals: 2874
bin: 3.75e1
variant carriers: 8

GenotypeDepth
all individuals: 1252
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 339
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8996
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35191
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2655
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4786
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2507
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 8
allele frequency: 6.962576153176675e-4
allele num: 11490
num of homozygotes: 0

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

East Asian
type: Population
allele count: 11
allele frequency: 1.27669452181987e-3
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.219809709685289e-4
allele num: 16396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.041917624870719e-5
allele num: 65748
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.181e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 1.933e0

VQSLOD
type: SiteQuality
SIO_000300: 2.55e0

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.37e-1

DP
type: SiteQuality
SIO_000300: 1.820333e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.07e-1

GenotypeDepth
all individuals: 875
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 221
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26032
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1235
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 727
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 819
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1518
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35271
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4776
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 246
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 590
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9071
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65776
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.933124755572937e-4
allele num: 10228
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.700191404210892e-4
allele num: 11494
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.218917601170161e-4
allele num: 16408
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.778e1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.05e-1

DP
type: SiteQuality
SIO_000300: 1.820406e6

FS
type: SiteQuality
SIO_000300: 1.826e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.879999999999999e-1

GenotypeDepth
all individuals: 257
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11784
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1157
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9074
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35479
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2669
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4764
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.093845216331505e-5
allele num: 16410
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 1.229e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.761e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.96e-1

DP
type: SiteQuality
SIO_000300: 1.821053e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
all individuals: 200
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 12370
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11839
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 166
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 192
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 820
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 339
bin: 5.75e1
variant carriers: 4

GenotypeDepth
all individuals: 225
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4781
bin: 9.75e1
variant carriers: 44

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2658
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2512
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36119
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9065
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 1.65188662841245e-3
allele num: 11502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 22
allele frequency: 3.339810541656546e-4
allele num: 65872
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.951981260979895e-4
allele num: 10246
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.68e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

FS
type: SiteQuality
SIO_000300: 1.093e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.283e1

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

DP
type: SiteQuality
SIO_000300: 1.830288e6

GenotypeDepth
all individuals: 653
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12429
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 656
bin: 4.75e1
variant carriers: 3

GenotypeDepth
all individuals: 1227
bin: 4.25e1
variant carriers: 8

GenotypeDepth
all individuals: 819
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 225
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 698
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36384
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4767
bin: 9.75e1
variant carriers: 34

GenotypeQuality
all individuals: 303
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9105
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65890
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.951981260979895e-4
allele num: 10246
num of homozygotes: 0

Latino
type: Population
allele count: 32
allele frequency: 2.782124847852547e-3
allele num: 11502
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.205e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 1.830547e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 1220
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 655
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 644
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26635
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2834
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9095
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4733
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36577
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2650
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
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: 1.516852228255923e-5
allele num: 65926
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6292
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.735e1

VQSLOD
type: SiteQuality
SIO_000300: -1.807e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e0

FS
type: SiteQuality
SIO_000300: 7.319e0

DP
type: SiteQuality
SIO_000300: 1.831037e6

QD
type: SiteQuality
SIO_000300: 7.08e0

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.45e-1

GenotypeDepth
all individuals: 11846
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26705
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 665
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 652
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2827
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 604
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1219
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36923
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9124
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4733
bin: 9.75e1
variant carriers: 2

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.946661475569399e-4
allele num: 10274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65972
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6294
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
SIO_000300: -2.3e0

MQRankSum
type: SiteQuality
SIO_000300: 2.37e0

MQ
type: SiteQuality
SIO_000300: 5.893e1

FS
type: SiteQuality
SIO_000300: 2.482e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

DP
type: SiteQuality
SIO_000300: 1.833874e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

GenotypeDepth
all individuals: 11817
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 652
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 26910
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2814
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1216
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 526
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37387
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2610
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4729
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2501
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9142
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1497
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.75e1
variant carriers: 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: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-5
allele num: 66060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6314
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.837211e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

MQ
type: SiteQuality
SIO_000300: 5.887e1

VQSLOD
type: SiteQuality
SIO_000300: -1.725e-1

QD
type: SiteQuality
SIO_000300: 1.171e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.81e-1

GenotypeDepth
all individuals: 168
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26929
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 652
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1216
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9133
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2485
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1498
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37507
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4728
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66082
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6308
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.942e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-1

DP
type: SiteQuality
SIO_000300: 1.837694e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.22e-1

FS
type: SiteQuality
SIO_000300: 1.385e0

QD
type: SiteQuality
SIO_000300: 1.472e1

GenotypeDepth
all individuals: 1917
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11860
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11602
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2779
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 819
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4711
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1937
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8773
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35731
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 565
bin: 8.75e1
variant carriers: 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: 1.520218911523259e-5
allele num: 65780
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.164144353899884e-4
allele num: 8590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6204
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.729050279329609e-5
allele num: 11456
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.869e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

QD
type: SiteQuality
SIO_000300: 1.432e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.897e0

MQRankSum
type: SiteQuality
SIO_000300: 6.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 1.810011e6

GenotypeDepth
all individuals: 1209
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 871
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2785
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 819
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4707
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 183
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8735
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2346
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6202
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521051350693599e-5
allele num: 65744
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.132e0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

DP
type: SiteQuality
SIO_000300: 1.80843e6

MQ
type: SiteQuality
SIO_000300: 5.748e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.149e1

GenotypeDepth
all individuals: 943
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2756
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 819
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1196
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25660
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2426
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8535
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2369
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4701
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2290
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35164
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6174
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522487134983709e-5
allele num: 65682
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.207e1

VQSLOD
type: SiteQuality
SIO_000300: 7.86e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.497e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.02e-1

DP
type: SiteQuality
SIO_000300: 1.797086e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 820
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9991
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23639
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 200
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3885
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4685
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2310
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1680
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2147
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31410
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8030
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65364
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.912556494399686e-4
allele num: 10178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6132
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.284e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

DP
type: SiteQuality
SIO_000300: 1.744405e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.752e0

GenotypeDepth
all individuals: 7075
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1173
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4073
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2801
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 490
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4676
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5099
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28830
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1749
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2068
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7037
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6084
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.812125484666901e-5
allele num: 11348
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.91e-1

DP
type: SiteQuality
SIO_000300: 1.690641e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 1.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-2

QD
type: SiteQuality
SIO_000300: 1.32e1

GenotypeDepth
all individuals: 1404
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9101
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9036
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 636
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6244
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22407
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1130
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1983
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1778
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4946
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3047
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6231
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4666
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.863676653075696e-5
allele num: 11282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5998
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.138e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -8.57e-1

QD
type: SiteQuality
SIO_000300: 1.697e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

DP
type: SiteQuality
SIO_000300: 1.610849e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.264e0

GenotypeDepth
all individuals: 2541
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1456
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6661
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 820
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8784
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4576
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3308
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20137
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6377
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5526
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 515
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1943
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5907
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4666
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5988
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.980982567353407e-4
allele num: 10096
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.862e0

VQSLOD
type: SiteQuality
SIO_000300: 4.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

DP
type: SiteQuality
SIO_000300: 1.587467e6

QD
type: SiteQuality
SIO_000300: 1.257e1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.328e0

GenotypeDepth
all individuals: 202
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12927
bin: 2.25e1
variant carriers: 66

GenotypeDepth
all individuals: 461
bin: 5.25e1
variant carriers: 4

GenotypeDepth
all individuals: 196
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 251
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 4

GenotypeDepth
all individuals: 14867
bin: 1.75e1
variant carriers: 62

GenotypeDepth
all individuals: 853
bin: 9.75e1
variant carriers: 49

GenotypeQuality
all individuals: 8791
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7246
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2968
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 632
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3340
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3511
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1194
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3725
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 786
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 445
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5535
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1720
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 507
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4914
bin: 9.75e1
variant carriers: 313

GenotypeQuality
all individuals: 1321
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 6681
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5864
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 11
allele frequency: 1.923076923076923e-3
allele num: 5720
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8254
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.588516746411483e-3
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.143171460003143e-5
allele num: 63630
num of homozygotes: 0

African
type: Population
allele count: 304
allele frequency: 3.059581320450886e-2
allele num: 9936
num of homozygotes: 9

South Asian
type: Population
allele count: 1
allele frequency: 6.261740763932373e-5
allele num: 15970
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.358695652173913e-3
allele num: 11040
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.444e1

MQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

VQSLOD
type: SiteQuality
SIO_000300: 6.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.490434e6

GenotypeDepth
all individuals: 472
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2380
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3882
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 556
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4332
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2505
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 239
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

African
type: Population
allele count: 19
allele frequency: 8.444444444444444e-3
allele num: 2250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7006
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.27e-2

QD
type: SiteQuality
SIO_000300: 1.281e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.739e0

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

FS
type: SiteQuality
SIO_000300: 1.697e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 3.0432e5

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 293
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2585
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 252
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 262
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3090
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4868
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3574
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 879
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.813953488372093e-3
allele num: 172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.224e0

DP
type: SiteQuality
SIO_000300: 3.12888e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.98e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.115e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.445e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

QD
type: SiteQuality
SIO_000300: 1.099e1

GenotypeDepth
all individuals: 1834
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1341
bin: 2.25e1
variant carriers: 5

GenotypeDepth
all individuals: 38
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 897
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 158
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 87
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3139
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5388
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 531
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3354
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1498
bin: 9.75e1
variant carriers: 19

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

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.210653753026634e-3
allele num: 7434
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 8.347245409015025e-4
allele num: 2396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 2.15311004784689e-2
allele num: 418
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.51e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.73e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

QD
type: SiteQuality
SIO_000300: 1.396e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

DP
type: SiteQuality
SIO_000300: 3.18671e5

GenotypeDepth
all individuals: 1422
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 483
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8654
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2750
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2943
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5697
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3475
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.278772378516624e-4
allele num: 7820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7476
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.306e0

QD
type: SiteQuality
SIO_000300: 1.017e1

DP
type: SiteQuality
SIO_000300: 3.20431e5

VQSLOD
type: SiteQuality
SIO_000300: -6.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.42e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

FS
type: SiteQuality
SIO_000300: 1.478e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.82e-2

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 135
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 446
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6823
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3798
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1403
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2229
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 541
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7834
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.293577981651376e-3
allele num: 436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.409999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.06e-1

QD
type: SiteQuality
SIO_000300: 1.373e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.36e-1

FS
type: SiteQuality
SIO_000300: 2.717e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 3.28571e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.78e-2

GenotypeDepth
all individuals: 907
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 193
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 159
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10469
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2931
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1461
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 88
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9091
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1495
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4196
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.546473134708429e-4
allele num: 7854
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.517e0

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.07e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.954e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.614e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e0

QD
type: SiteQuality
SIO_000300: 1.119e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

DP
type: SiteQuality
SIO_000300: 3.39425e5

GenotypeDepth
all individuals: 159
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2944
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 761
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 905
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 192
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4215
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1467
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9478
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.24595066035385e-4
allele num: 8026
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.19e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.148e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 3.40512e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

QD
type: SiteQuality
SIO_000300: 1.085e1

GenotypeDepth
all individuals: 159
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 9.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 440
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 300
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1952
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4446
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1500
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11909
bin: 7.5e0
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.532928064842959e-4
allele num: 7896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.108e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.92e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

DP
type: SiteQuality
SIO_000300: 3.56748e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.163e-1

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 489
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 119
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 424
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13716
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 191
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12265
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4561
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.836e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 5.575e1

DP
type: SiteQuality
SIO_000300: 3.57504e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.97e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.386e1

GenotypeDepth
all individuals: 293
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2415
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3136
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 926
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1985
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 366
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1748
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 587
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11539
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1524
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 671
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1493
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4684
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 7.27802037845706e-4
allele num: 2748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.607e0

MQ
type: SiteQuality
SIO_000300: 5.989e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.26e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

FS
type: SiteQuality
SIO_000300: 2.234e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e0

MQRankSum
type: SiteQuality
SIO_000300: 1.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.98e-2

DP
type: SiteQuality
SIO_000300: 3.57202e5

GenotypeDepth
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2388
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3150
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 135
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1985
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 384
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10786
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2025
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 669
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.152604887044721e-4
allele num: 8676
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.381e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.64e0

DP
type: SiteQuality
SIO_000300: 3.56036e5

MQRankSum
type: SiteQuality
SIO_000300: -8.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.82e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.514e1

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3148
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 489
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1984
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1530
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10816
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4689
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.152604887044721e-4
allele num: 8676
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.73e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.067e-1

QD
type: SiteQuality
SIO_000300: 1.483e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e0

DP
type: SiteQuality
SIO_000300: 3.56269e5

MQRankSum
type: SiteQuality
SIO_000300: -3.05e-1

MQ
type: SiteQuality
SIO_000300: 5.828e1

GenotypeDepth
all individuals: 104
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 144
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1963
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 293
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 572
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11488
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4401
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2744
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.270325203252033e-4
allele num: 7872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.55314e5

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e0

QD
type: SiteQuality
SIO_000300: 1.285e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.78e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.993e0

FS
type: SiteQuality
SIO_000300: 3.627e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.091e0

GenotypeDepth
all individuals: 196
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2244
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10952
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1500
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 502
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.274534794799898e-4
allele num: 7846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.44e0

DP
type: SiteQuality
SIO_000300: 3.51644e5

QD
type: SiteQuality
SIO_000300: 1.401e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 5.25e1
variant carriers: 3

GenotypeDepth
all individuals: 104
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 51
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 918
bin: 3.75e1
variant carriers: 3

GenotypeDepth
all individuals: 67
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10952
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 222
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2244
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1500
bin: 9.75e1
variant carriers: 21

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2744
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.631578947368421e-3
allele num: 380
num of homozygotes: 0

South Asian
type: Population
allele count: 21
allele frequency: 2.676523069079786e-3
allele num: 7846
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

QD
type: SiteQuality
SIO_000300: 1.401e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.44e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.51644e5

GenotypeDepth
all individuals: 682
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 872
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 293
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2213
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 4843
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 228
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8832
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 465
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1038
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.061821613968853e-3
allele num: 8476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 5.3475935828877e-3
allele num: 374
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.102e0

MQRankSum
type: SiteQuality
SIO_000300: -4.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.519999999999999e-2

FS
type: SiteQuality
SIO_000300: 1.837e0

DP
type: SiteQuality
SIO_000300: 3.37029e5

QD
type: SiteQuality
SIO_000300: 1.119e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.28e-1

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2099
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 193
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2236
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4573
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9164
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2568
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 466
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7766
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.645502645502645e-3
allele num: 378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

DP
type: SiteQuality
SIO_000300: 3.36965e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.419999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.071e0

MQRankSum
type: SiteQuality
SIO_000300: -7.96e-1

QD
type: SiteQuality
SIO_000300: 2.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
SIO_000300: -3.969e0

GenotypeDepth
all individuals: 3873
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6920
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 924
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4334
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 633
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3809
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2495
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5374
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4235
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1906
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4326
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5260
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 24223
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9356
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.619957881095092e-5
allele num: 61730
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.540222367560497e-5
allele num: 15290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10584
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.727e-1

MQ
type: SiteQuality
SIO_000300: 5.896e1

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.747e0

DP
type: SiteQuality
SIO_000300: 1.469042e6

QD
type: SiteQuality
SIO_000300: 3.462e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

FS
type: SiteQuality
SIO_000300: 7.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

GenotypeDepth
all individuals: 3932
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1330
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3227
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5260
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 414
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5182
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27967
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1381
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3887
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8118
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.307360439273108e-4
allele num: 15298
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10666
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9398
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.529e1

VQSLOD
type: SiteQuality
SIO_000300: -6.11e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

DP
type: SiteQuality
SIO_000300: 1.503387e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.821e0

GenotypeDepth
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7698
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1326
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4000
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2883
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29825
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5260
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 713
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5138
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.609476598210262e-5
allele num: 62132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.98e-1

FS
type: SiteQuality
SIO_000300: 4.869e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.52e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 1.346e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 1.514988e6

GenotypeDepth
all individuals: 292
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 226
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1324
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1780
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30233
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5028
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3072
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2643
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5262
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1016
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4061
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5788
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10700
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8156
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.05977108944468e-4
allele num: 9436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15344
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.5215e6

QD
type: SiteQuality
SIO_000300: 1.108e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.43e-1

GenotypeDepth
all individuals: 12057
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4013
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 1778
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4113
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5263
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4954
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2897
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31616
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10722
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15362
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 5.72e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.233e0

FS
type: SiteQuality
SIO_000300: 2.808e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 1.530128e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

GenotypeDepth
all individuals: 226
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12256
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 293
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 340
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4785
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5264
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 283
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2545
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33390
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1900
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5838
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.504488096786782e-5
allele num: 15374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9474
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.218323586744639e-4
allele num: 8208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10762
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e0

FS
type: SiteQuality
SIO_000300: 3.852e0

MQRankSum
type: SiteQuality
SIO_000300: 8.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.382e-1

DP
type: SiteQuality
SIO_000300: 1.544882e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.879e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 9.23e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

GenotypeDepth
all individuals: 5762
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 226
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1322
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12338
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4699
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 594
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4192
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1323
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1754
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2391
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33961
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5264
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.596424010217114e-5
allele num: 62640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

QD
type: SiteQuality
SIO_000300: 1.27e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.338e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.037e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.338e0

FS
type: SiteQuality
SIO_000300: 3.841e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.73e-1

DP
type: SiteQuality
SIO_000300: 1.549936e6

GenotypeDepth
all individuals: 5389
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1325
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1781
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4595
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1328
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5264
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2213
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34627
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4206
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5870
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.212121212121212e-4
allele num: 8250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62728
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.072e0

FS
type: SiteQuality
SIO_000300: 3.197e0

DP
type: SiteQuality
SIO_000300: 1.556578e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.507e0

MQ
type: SiteQuality
SIO_000300: 5.811e1

QD
type: SiteQuality
SIO_000300: 9.17e0

GenotypeDepth
all individuals: 4226
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 550
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 97
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 635
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 926
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13781
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4510
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5269
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39991
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3295
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1398
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562695336917115e-5
allele num: 63992
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQRankSum
type: SiteQuality
SIO_000300: 4.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.09e0

DP
type: SiteQuality
SIO_000300: 1.62095e6

VQSLOD
type: SiteQuality
SIO_000300: -7.209e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

GenotypeDepth
all individuals: 14030
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 443
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 88
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4238
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1716
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1327
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1800
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 926
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5267
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 227
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40679
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3090
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4545
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.018744906275469e-4
allele num: 9816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11094
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.886e0

VQSLOD
type: SiteQuality
SIO_000300: -3.552e0

MQRankSum
type: SiteQuality
SIO_000300: -1.184e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.901e1

DP
type: SiteQuality
SIO_000300: 1.629577e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.009e0

FS
type: SiteQuality
SIO_000300: 9.615e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e0

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1539
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30099
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1326
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1801
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5268
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 247
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1257
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3041
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4613
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40775
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15748
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551734839550618e-5
allele num: 64444
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.876e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 8.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.855e1

DP
type: SiteQuality
SIO_000300: 1.639732e6

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1645
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 928
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29769
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3199
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40453
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1436
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4600
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5268
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 377
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.016053647632595e-4
allele num: 9842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11128
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64416
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15740
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6138
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.43e-1

FS
type: SiteQuality
SIO_000300: 1.77e0

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.054e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.157e0

DP
type: SiteQuality
SIO_000300: 1.63854e6

QD
type: SiteQuality
SIO_000300: 1.148e1

GenotypeDepth
all individuals: 928
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1325
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15252
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27666
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4422
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1210
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4469
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39535
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5266
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11024
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.419309282321222e-5
allele num: 15578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64010
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

DP
type: SiteQuality
SIO_000300: 1.624315e6

FS
type: SiteQuality
SIO_000300: 1.922e0

VQSLOD
type: SiteQuality
SIO_000300: 2.06e-1

QD
type: SiteQuality
SIO_000300: 8.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.92e-1

GenotypeDepth
all individuals: 4213
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4075
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1325
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 926
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21818
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 226
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14527
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7096
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33283
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1499
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 354
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8479
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1623
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3985
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5266
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15086
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.197135366711427e-5
allele num: 62556
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.552105e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

QD
type: SiteQuality
SIO_000300: 8.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

GenotypeDepth
all individuals: 4449
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1327
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30602
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9871
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 923
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3819
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5265
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 415
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.61025409809668e-5
allele num: 62102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14962
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 1.520145e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.586e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.381999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.386e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.371e0

QD
type: SiteQuality
SIO_000300: 6.54e0