2-70919547-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919547
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919547
    reference: chr 2
allele count: 5
allele frequency: 4.577077993409007e-5
allele num: 109240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.693G>A
  hgvsp: ENST00000456320.3:c.693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.741G>A
  hgvsp: ENST00000430656.1:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.693G>A
  hgvsp: ENST00000264436.4:c.693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.693G>A
  hgvsp: ENST00000413157.2:c.693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+132G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.693G>A
  hgvsp: ENST00000403045.2:c.693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.693G>A
  hgvsp: ENST00000355733.3:c.693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.693G>A
  hgvsp: ENST00000407644.2:c.693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12540
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35479
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1545
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6536
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro231Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

2-70919561-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919561
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919561
    reference: chr 2
allele count: 16
allele frequency: 1.435750179468773e-4
allele num: 111440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.679C>A
  hgvsp: ENSP00000384303.2:p.His227Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.679C>A
  hgvsp: ENSP00000414546.3:p.His227Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.679C>A
  hgvsp: ENSP00000264436.3:p.His227Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.679C>A
  hgvsp: ENSP00000347972.3:p.His227Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.679C>A
  hgvsp: ENSP00000384677.2:p.His227Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.679C>A
  hgvsp: ENST00000415348.1:c.679C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+118C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.727C>A
  hgvsp: ENSP00000398112.1:p.His243Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.679C>A
  hgvsp: ENSP00000388072.2:p.His227Asn
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13299
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28603
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His227Asn
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP

2-70919572-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919572
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919572
    reference: chr 2
allele count: 1
allele frequency: 8.854886126164418e-6
allele num: 112932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.668G>A
  hgvsp: ENSP00000347972.3:p.Arg223His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.668G>A
  hgvsp: ENSP00000414546.3:p.Arg223His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.668G>A
  hgvsp: ENSP00000264436.3:p.Arg223His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.668G>A
  hgvsp: ENSP00000384677.2:p.Arg223His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.716G>A
  hgvsp: ENSP00000398112.1:p.Arg239His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+107G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.668G>A
  hgvsp: ENSP00000412357.1:p.Arg223His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.668G>A
  hgvsp: ENSP00000384303.2:p.Arg223His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.668G>A
  hgvsp: ENSP00000388072.2:p.Arg223His
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1454
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2206
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg223His
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ

2-70919576-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919576
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919576
    reference: chr 2
allele count: 1
allele frequency: 8.77654906090925e-6
allele num: 113940
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.664G>A
  hgvsp: ENSP00000384677.2:p.Val222Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.664G>A
  hgvsp: ENSP00000384303.2:p.Val222Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.664G>A
  hgvsp: ENSP00000264436.3:p.Val222Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.664G>A
  hgvsp: ENSP00000388072.2:p.Val222Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.664G>A
  hgvsp: ENSP00000347972.3:p.Val222Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.664G>A
  hgvsp: ENSP00000412357.1:p.Val222Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.664G>A
  hgvsp: ENSP00000414546.3:p.Val222Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+103G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.712G>A
  hgvsp: ENSP00000398112.1:p.Val238Met
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27821
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1841
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val222Met
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

2-70919577-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919577
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919577
    reference: chr 2
allele count: 3
allele frequency: 2.623111359820929e-5
allele num: 114368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.663C>T
  hgvsp: ENST00000415348.1:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.663C>T
  hgvsp: ENST00000407644.2:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+102C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.663C>T
  hgvsp: ENST00000403045.2:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.663C>T
  hgvsp: ENST00000264436.4:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.711C>T
  hgvsp: ENST00000430656.1:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.663C>T
  hgvsp: ENST00000355733.3:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.663C>T
  hgvsp: ENST00000456320.3:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.663C>T
  hgvsp: ENST00000413157.2:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14307
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4943
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp221Asp
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

2-70919579-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919579
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919579
    reference: chr 2
allele count: 2
allele frequency: 1.74440916861459e-5
allele num: 114652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.661G>A
  hgvsp: ENSP00000384677.2:p.Asp221Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.661G>A
  hgvsp: ENSP00000412357.1:p.Asp221Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.661G>A
  hgvsp: ENSP00000388072.2:p.Asp221Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.661G>A
  hgvsp: ENSP00000264436.3:p.Asp221Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.661G>A
  hgvsp: ENSP00000347972.3:p.Asp221Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.709G>A
  hgvsp: ENSP00000398112.1:p.Asp237Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.661G>A
  hgvsp: ENSP00000414546.3:p.Asp221Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+100G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.661G>A
  hgvsp: ENSP00000384303.2:p.Asp221Asn
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14437
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28351
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5083
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4657
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp221Asn
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

2-70919581-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919581
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919581
    reference: chr 2
allele count: 2
allele frequency: 1.734124093920161e-5
allele num: 115332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.659C>T
  hgvsp: ENSP00000384303.2:p.Pro220Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.659C>T
  hgvsp: ENSP00000264436.3:p.Pro220Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.659C>T
  hgvsp: ENSP00000414546.3:p.Pro220Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.707C>T
  hgvsp: ENSP00000398112.1:p.Pro236Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+98C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.659C>T
  hgvsp: ENSP00000347972.3:p.Pro220Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.659C>T
  hgvsp: ENSP00000412357.1:p.Pro220Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.659C>T
  hgvsp: ENSP00000384677.2:p.Pro220Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.659C>T
  hgvsp: ENSP00000388072.2:p.Pro220Leu
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14488
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro220Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

2-70919586-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919586
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919586
    reference: chr 2
allele count: 1
allele frequency: 8.618163641691228e-6
allele num: 116034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.702G>A
  hgvsp: ENST00000430656.1:c.702G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.654G>A
  hgvsp: ENST00000456320.3:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.654G>A
  hgvsp: ENST00000355733.3:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.654G>A
  hgvsp: ENST00000264436.4:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+93G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.654G>A
  hgvsp: ENST00000413157.2:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.654G>A
  hgvsp: ENST00000415348.1:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.654G>A
  hgvsp: ENST00000407644.2:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.654G>A
  hgvsp: ENST00000403045.2:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala218Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

2-70919587-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919587
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919587
    reference: chr 2
allele count: 2
allele frequency: 1.721763085399449e-5
allele num: 116160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.653C>T
  hgvsp: ENSP00000384677.2:p.Ala218Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.653C>T
  hgvsp: ENSP00000388072.2:p.Ala218Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.653C>T
  hgvsp: ENSP00000384303.2:p.Ala218Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.653C>T
  hgvsp: ENSP00000347972.3:p.Ala218Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.701C>T
  hgvsp: ENSP00000398112.1:p.Ala234Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.653C>T
  hgvsp: ENSP00000412357.1:p.Ala218Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.653C>T
  hgvsp: ENSP00000414546.3:p.Ala218Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.653C>T
  hgvsp: ENSP00000264436.3:p.Ala218Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+92C>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1531
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala218Val
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

2-70919589-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919589
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919589
    reference: chr 2
allele count: 9
allele frequency: 7.707459107647512e-5
allele num: 116770
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.651A>G
  hgvsp: ENST00000264436.4:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.651A>G
  hgvsp: ENST00000456320.3:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.651A>G
  hgvsp: ENST00000403045.2:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.651A>G
  hgvsp: ENST00000407644.2:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+90A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.651A>G
  hgvsp: ENST00000355733.3:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.699A>G
  hgvsp: ENST00000430656.1:c.699A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.651A>G
  hgvsp: ENST00000415348.1:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.651A>G
  hgvsp: ENST00000413157.2:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15027
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37870
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3696
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala217Ala
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

2-70919589-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919589
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919589
    reference: chr 2
allele count: 1
allele frequency: 8.56384345294168e-6
allele num: 116770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.651A>C
  hgvsp: ENST00000413157.2:c.651A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.651A>C
  hgvsp: ENST00000403045.2:c.651A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.651A>C
  hgvsp: ENST00000355733.3:c.651A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.651A>C
  hgvsp: ENST00000415348.1:c.651A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.651A>C
  hgvsp: ENST00000264436.4:c.651A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.651A>C
  hgvsp: ENST00000456320.3:c.651A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.699A>C
  hgvsp: ENST00000430656.1:c.699A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+90A>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.651A>C
  hgvsp: ENST00000407644.2:c.651A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1533
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala217Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

2-70919592-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919592
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919592
    reference: chr 2
allele count: 2
allele frequency: 1.708233686368295e-5
allele num: 117080
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.648T>C
  hgvsp: ENST00000264436.4:c.648T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.648T>C
  hgvsp: ENST00000403045.2:c.648T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.648T>C
  hgvsp: ENST00000355733.3:c.648T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+87T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.648T>C
  hgvsp: ENST00000456320.3:c.648T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.696T>C
  hgvsp: ENST00000430656.1:c.696T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.648T>C
  hgvsp: ENST00000407644.2:c.648T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.648T>C
  hgvsp: ENST00000415348.1:c.648T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.648T>C
  hgvsp: ENST00000413157.2:c.648T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1429
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr216Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

2-70919597-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919597
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919597
    reference: chr 2
allele count: 2
allele frequency: 1.702736297229648e-5
allele num: 117458
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+82A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.643A>G
  hgvsp: ENSP00000388072.2:p.Ile215Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.643A>G
  hgvsp: ENSP00000347972.3:p.Ile215Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.691A>G
  hgvsp: ENSP00000398112.1:p.Ile231Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.643A>G
  hgvsp: ENSP00000384303.2:p.Ile215Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.643A>G
  hgvsp: ENSP00000414546.3:p.Ile215Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.643A>G
  hgvsp: ENSP00000384677.2:p.Ile215Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.643A>G
  hgvsp: ENSP00000412357.1:p.Ile215Val
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.643A>G
  hgvsp: ENSP00000264436.3:p.Ile215Val
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38161
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile215Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

2-70919601-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919601
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919601
    reference: chr 2
allele count: 5
allele frequency: 4.25105000935231e-5
allele num: 117618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.639G>A
  hgvsp: ENST00000403045.2:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+78G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.639G>A
  hgvsp: ENST00000415348.1:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.639G>A
  hgvsp: ENST00000355733.3:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.639G>A
  hgvsp: ENST00000264436.4:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.639G>A
  hgvsp: ENST00000407644.2:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.639G>A
  hgvsp: ENST00000413157.2:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.687G>A
  hgvsp: ENST00000430656.1:c.687G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.639G>A
  hgvsp: ENST00000456320.3:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15767
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30326
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser213Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

2-70919602-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919602
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919602
    reference: chr 2
allele count: 3
allele frequency: 2.54911290870777e-5
allele num: 117688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.638C>T
  hgvsp: ENSP00000384303.2:p.Ser213Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.638C>T
  hgvsp: ENSP00000384677.2:p.Ser213Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.638C>T
  hgvsp: ENSP00000412357.1:p.Ser213Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.638C>T
  hgvsp: ENSP00000414546.3:p.Ser213Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.686C>T
  hgvsp: ENSP00000398112.1:p.Ser229Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.638C>T
  hgvsp: ENSP00000347972.3:p.Ser213Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.638C>T
  hgvsp: ENSP00000264436.3:p.Ser213Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.638C>T
  hgvsp: ENSP00000388072.2:p.Ser213Leu
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+77C>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30361
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15917
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser213Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

2-70919611-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919611
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919611
    reference: chr 2
allele count: 1
allele frequency: 8.461668641056017e-6
allele num: 118180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.677G>C
  hgvsp: ENSP00000398112.1:p.Cys226Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.629G>C
  hgvsp: ENSP00000384303.2:p.Cys210Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.629G>C
  hgvsp: ENSP00000384677.2:p.Cys210Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.629G>C
  hgvsp: ENSP00000264436.3:p.Cys210Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.629G>C
  hgvsp: ENSP00000388072.2:p.Cys210Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.629G>C
  hgvsp: ENSP00000412357.1:p.Cys210Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+68G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.629G>C
  hgvsp: ENSP00000347972.3:p.Cys210Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.629G>C
  hgvsp: ENSP00000414546.3:p.Cys210Ser
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16460
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5626
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys210Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS

2-70919616-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919616
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919616
    reference: chr 2
allele count: 10
allele frequency: 8.447372867038352e-5
allele num: 118380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.624C>T
  hgvsp: ENST00000407644.2:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.624C>T
  hgvsp: ENST00000456320.3:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.624C>T
  hgvsp: ENST00000264436.4:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.624C>T
  hgvsp: ENST00000403045.2:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.672C>T
  hgvsp: ENST00000430656.1:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.624C>T
  hgvsp: ENST00000355733.3:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.624C>T
  hgvsp: ENST00000413157.2:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+63C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.624C>T
  hgvsp: ENST00000415348.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16746
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly208Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

2-70919621-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919621
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919621
    reference: chr 2
allele count: 2
allele frequency: 1.687991627561527e-5
allele num: 118484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.619A>T
  hgvsp: ENSP00000412357.1:p.Thr207Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.619A>T
  hgvsp: ENSP00000384303.2:p.Thr207Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.619A>T
  hgvsp: ENSP00000264436.3:p.Thr207Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.619A>T
  hgvsp: ENSP00000347972.3:p.Thr207Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.619A>T
  hgvsp: ENSP00000414546.3:p.Thr207Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.619A>T
  hgvsp: ENSP00000388072.2:p.Thr207Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+58A>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.667A>T
  hgvsp: ENSP00000398112.1:p.Thr223Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.619A>T
  hgvsp: ENSP00000384677.2:p.Thr207Ser
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2470
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr207Ser
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

2-70919633-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919633
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919633
    reference: chr 2
allele count: 1
allele frequency: 8.430565859580495e-6
allele num: 118616
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.607C>T
  hgvsp: ENSP00000264436.3:p.Pro203Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.607C>T
  hgvsp: ENSP00000388072.2:p.Pro203Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.607C>T
  hgvsp: ENSP00000347972.3:p.Pro203Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.607C>T
  hgvsp: ENSP00000414546.3:p.Pro203Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.607C>T
  hgvsp: ENSP00000384677.2:p.Pro203Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.655C>T
  hgvsp: ENSP00000398112.1:p.Pro219Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.607C>T
  hgvsp: ENSP00000412357.1:p.Pro203Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.607C>T
  hgvsp: ENSP00000384303.2:p.Pro203Ser
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+46C>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42214
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2251
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5906
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro203Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

2-70919641-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919641
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919641
    reference: chr 2
allele count: 1
allele frequency: 8.440385556812235e-6
allele num: 118478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+38G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.599G>A
  hgvsp: ENSP00000412357.1:p.Ser200Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.599G>A
  hgvsp: ENSP00000384677.2:p.Ser200Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.599G>A
  hgvsp: ENSP00000264436.3:p.Ser200Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.599G>A
  hgvsp: ENSP00000347972.3:p.Ser200Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.599G>A
  hgvsp: ENSP00000388072.2:p.Ser200Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.599G>A
  hgvsp: ENSP00000414546.3:p.Ser200Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.647G>A
  hgvsp: ENSP00000398112.1:p.Ser216Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.599G>A
  hgvsp: ENSP00000384303.2:p.Ser200Asn
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser200Asn
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-70919670-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919670
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919670
    reference: chr 2
allele count: 1
allele frequency: 8.612077577594818e-6
allele num: 116116
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.570T>C
  hgvsp: ENST00000355733.3:c.570T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.570T>C
  hgvsp: ENST00000413157.2:c.570T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.570T>C
  hgvsp: ENST00000456320.3:c.570T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.570T>C
  hgvsp: ENST00000407644.2:c.570T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.570T>C
  hgvsp: ENST00000415348.1:c.570T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.570T>C
  hgvsp: ENST00000264436.4:c.570T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+9T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.618T>C
  hgvsp: ENST00000430656.1:c.618T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.570T>C
  hgvsp: ENST00000403045.2:c.570T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18583
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile190Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

2-70919678-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919678
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919678
    reference: chr 2
allele count: 2
allele frequency: 1.7373477649021e-5
allele num: 115118
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.562G>A
  hgvsp: ENSP00000264436.3:p.Val188Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.561+1G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.562G>A
  hgvsp: ENSP00000414546.3:p.Val188Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.562G>A
  hgvsp: ENSP00000384303.2:p.Val188Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.562G>A
  hgvsp: ENSP00000384677.2:p.Val188Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.562G>A
  hgvsp: ENSP00000412357.1:p.Val188Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.610G>A
  hgvsp: ENSP00000398112.1:p.Val204Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.562G>A
  hgvsp: ENSP00000347972.3:p.Val188Met
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.562G>A
  hgvsp: ENSP00000388072.2:p.Val188Met
  variant of: http://identifiers.org/hgnc/244
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18430
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40589
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 5.25e1
  variant carriers: 0
hgvs: c.561+1G>A
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

2-70919688-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919688
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919688
    reference: chr 2
allele count: 3
allele frequency: 2.633149598005828e-5
allele num: 113932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-4G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-4G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-4G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-4G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-4G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-4G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-4G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-4G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-4G>A
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18239
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
hgvs: c.556-4G>A
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: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

2-70919689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919689
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919689
    reference: chr 2
allele count: 2
allele frequency: 1.756327168624971e-5
allele num: 113874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-5C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-5C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-5C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-5C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-5C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-5C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-5C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-5C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-5C>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27399
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
hgvs: c.556-5C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

2-70919691-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919691
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919691
    reference: chr 2
allele count: 1
allele frequency: 8.802506953980493e-6
allele num: 113604
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-7G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-7G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-7G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-7G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-7G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-7G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-7G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-7G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-7G>C
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 7.5e0
  variant carriers: 0
hgvs: c.556-7G>C
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

2-70919704-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919704
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919704
    reference: chr 2
allele count: 43
allele frequency: 3.829165776162998e-4
allele num: 112296
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-20T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-20T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-20T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-20T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-20T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-20T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-20T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-20T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-20T>C
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17650
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25059
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1530
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5234
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 2
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

2-70919708-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919708
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919708
    reference: chr 2
allele count: 1
allele frequency: 8.942944017170453e-6
allele num: 111820
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-24A>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-24A>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-24A>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-24A>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-24A>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-24A>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-24A>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-24A>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-24A>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

2-70919710-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919710
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919710
    reference: chr 2
allele count: 1
allele frequency: 8.958325868061777e-6
allele num: 111628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-26T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-26T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-26T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-26T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-26T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-26T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-26T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-26T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-26T>A
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17038
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

2-70919711-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919711
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919711
    reference: chr 2
allele count: 1
allele frequency: 8.969253399347038e-6
allele num: 111492
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-27A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-27A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-27A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-27A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-27A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-27A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-27A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-27A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-27A>G
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22613
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1809
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6783
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

2-70919720-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919720
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919720
    reference: chr 2
allele count: 3
allele frequency: 2.744186897422294e-5
allele num: 109322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-36C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-36C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-36C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-36C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-36C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-36C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-36C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-36C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-36C>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9683
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1335
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS

2-70919722-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919722
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919722
    reference: chr 2
allele count: 1
allele frequency: 9.163551059306502e-6
allele num: 109128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-38A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-38A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-38A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-38A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-38A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-38A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-38A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-38A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-38A>G
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

2-70919726-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919726
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919726
    reference: chr 2
allele count: 170
allele frequency: 1.581571896397737e-3
allele num: 107488
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-42G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-42G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-42G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-42G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-42G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-42G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-42G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-42G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-42G>A
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8638
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13149
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 16811
  bin: 2.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10072
  bin: 2.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 3.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 3566
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3098
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5542
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

2-70919727-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919727
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919727
    reference: chr 2
allele count: 2
allele frequency: 1.861434793939168e-5
allele num: 107444
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-43C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-43C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-43C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-43C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-43C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-43C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-43C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-43C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-43C>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16846
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5897
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3717
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5552
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ

2-70919735-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70919735
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70919735
    reference: chr 2
allele count: 58
allele frequency: 5.498151483552944e-4
allele num: 105490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.556-51C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.556-51C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.556-51C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.604-51C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.556-51C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.556-51C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.556-51C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.556-51C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.556-51C>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 8927
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 18080
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 8560
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12905
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5034
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2186
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5531
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3102
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

2-70922812-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922812
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922812
    reference: chr 2
allele count: 1
allele frequency: 8.444519506840061e-6
allele num: 118420
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.555+41T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.555+41T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.555+41T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.555+41T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.555+41T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.603+41T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.555+41T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.555+41T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.555+41T>C
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35696
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

2-70922818-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922818
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922818
    reference: chr 2
allele count: 29
allele frequency: 2.443669211453225e-4
allele num: 118674
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.555+35T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.603+35T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.555+35T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.555+35T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.555+35T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.555+35T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.555+35T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.555+35T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.555+35T>C
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17177
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26535
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1744
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1808
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

2-70922827-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922827
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922827
    reference: chr 2
allele count: 82
allele frequency: 6.883814640698455e-4
allele num: 119120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.555+26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.555+26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.555+26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.603+26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.555+26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.555+26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.555+26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.555+26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.555+26C>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28142
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 18145
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6157
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-70922834-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922834
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922834
    reference: chr 2
allele count: 1
allele frequency: 8.36372152152822e-6
allele num: 119564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.555+19C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.555+19C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.555+19C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.555+19C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.603+19C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.555+19C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.555+19C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.555+19C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.555+19C>A
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43045
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

2-70922855-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922855
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922855
    reference: chr 2
allele count: 331
allele frequency: 2.746933559063221e-3
allele num: 120498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.553C>T
  hgvsp: ENST00000456320.3:c.553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.553C>T
  hgvsp: ENST00000403045.2:c.553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.553C>T
  hgvsp: ENST00000415348.1:c.553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.553C>T
  hgvsp: ENST00000355733.3:c.553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.553C>T
  hgvsp: ENST00000407644.2:c.553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.553C>T
  hgvsp: ENST00000264436.4:c.553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.601C>T
  hgvsp: ENST00000430656.1:c.601C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.553C>T
  hgvsp: ENST00000522886.1:c.553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.553C>T
  hgvsp: ENST00000413157.2:c.553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 19781
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 29474
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5487
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: c.553C>T
num of homozygotes: 5
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

2-70922857-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922857
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922857
    reference: chr 2
allele count: 1
allele frequency: 8.299306178003518e-6
allele num: 120492
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.551G>A
  hgvsp: ENSP00000264436.3:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.551G>A
  hgvsp: ENSP00000384303.2:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.551G>A
  hgvsp: ENSP00000347972.3:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.551G>A
  hgvsp: ENSP00000430243.1:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.551G>A
  hgvsp: ENSP00000414546.3:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.551G>A
  hgvsp: ENSP00000388072.2:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.551G>A
  hgvsp: ENSP00000384677.2:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.599G>A
  hgvsp: ENSP00000398112.1:p.Ser200Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.551G>A
  hgvsp: ENSP00000412357.1:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6507
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2751
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser184Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

2-70922862-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922862
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922862
    reference: chr 2
allele count: 14
allele frequency: 1.161266776157534e-4
allele num: 120558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.546G>A
  hgvsp: ENST00000456320.3:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.546G>A
  hgvsp: ENST00000407644.2:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.546G>A
  hgvsp: ENST00000355733.3:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.546G>A
  hgvsp: ENST00000522886.1:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.594G>A
  hgvsp: ENST00000430656.1:c.594G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.546G>A
  hgvsp: ENST00000264436.4:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.546G>A
  hgvsp: ENST00000403045.2:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.546G>A
  hgvsp: ENST00000413157.2:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.546G>A
  hgvsp: ENST00000415348.1:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20048
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29468
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6506
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala182Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

2-70922865-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922865
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922865
    reference: chr 2
allele count: 2
allele frequency: 1.658374792703151e-5
allele num: 120600
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.543A>G
  hgvsp: ENST00000355733.3:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.543A>G
  hgvsp: ENST00000264436.4:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.591A>G
  hgvsp: ENST00000430656.1:c.591A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.543A>G
  hgvsp: ENST00000407644.2:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.543A>G
  hgvsp: ENST00000415348.1:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.543A>G
  hgvsp: ENST00000456320.3:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.543A>G
  hgvsp: ENST00000403045.2:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.543A>G
  hgvsp: ENST00000413157.2:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.543A>G
  hgvsp: ENST00000522886.1:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5555
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6524
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr181Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-70922874-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922874
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922874
    reference: chr 2
allele count: 2
allele frequency: 1.658044833532299e-5
allele num: 120624
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.534T>G
  hgvsp: ENSP00000264436.3:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.534T>G
  hgvsp: ENSP00000414546.3:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.534T>G
  hgvsp: ENSP00000412357.1:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.534T>G
  hgvsp: ENSP00000430243.1:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.534T>G
  hgvsp: ENSP00000347972.3:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.534T>G
  hgvsp: ENSP00000384303.2:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.582T>G
  hgvsp: ENSP00000398112.1:p.Ser194Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.534T>G
  hgvsp: ENSP00000388072.2:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.534T>G
  hgvsp: ENSP00000384677.2:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser178Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

2-70922874-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922874
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922874
    reference: chr 2
allele count: 1
allele frequency: 8.290224167661493e-6
allele num: 120624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.534T>A
  hgvsp: ENSP00000430243.1:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.534T>A
  hgvsp: ENSP00000264436.3:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.534T>A
  hgvsp: ENSP00000412357.1:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.534T>A
  hgvsp: ENSP00000384677.2:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.534T>A
  hgvsp: ENSP00000414546.3:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.534T>A
  hgvsp: ENSP00000388072.2:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.582T>A
  hgvsp: ENSP00000398112.1:p.Ser194Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.534T>A
  hgvsp: ENSP00000347972.3:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.534T>A
  hgvsp: ENSP00000384303.2:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45031
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser178Arg
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

2-70922875-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922875
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922875
    reference: chr 2
allele count: 1
allele frequency: 8.290499088045101e-6
allele num: 120620
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.533G>A
  hgvsp: ENSP00000384303.2:p.Ser178Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.533G>A
  hgvsp: ENSP00000412357.1:p.Ser178Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.533G>A
  hgvsp: ENSP00000430243.1:p.Ser178Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.533G>A
  hgvsp: ENSP00000414546.3:p.Ser178Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.533G>A
  hgvsp: ENSP00000264436.3:p.Ser178Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.581G>A
  hgvsp: ENSP00000398112.1:p.Ser194Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.533G>A
  hgvsp: ENSP00000347972.3:p.Ser178Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.533G>A
  hgvsp: ENSP00000384677.2:p.Ser178Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.533G>A
  hgvsp: ENSP00000388072.2:p.Ser178Asn
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser178Asn
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-70922888-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922888
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922888
    reference: chr 2
allele count: 1
allele frequency: 8.292011476143882e-6
allele num: 120598
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.520G>C
  hgvsp: ENSP00000264436.3:p.Gly174Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.568G>C
  hgvsp: ENSP00000398112.1:p.Gly190Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.520G>C
  hgvsp: ENSP00000347972.3:p.Gly174Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.520G>C
  hgvsp: ENSP00000430243.1:p.Gly174Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.520G>C
  hgvsp: ENSP00000414546.3:p.Gly174Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.520G>C
  hgvsp: ENSP00000384677.2:p.Gly174Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.520G>C
  hgvsp: ENSP00000388072.2:p.Gly174Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.520G>C
  hgvsp: ENSP00000412357.1:p.Gly174Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.520G>C
  hgvsp: ENSP00000384303.2:p.Gly174Arg
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6496
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly174Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

2-70922896-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922896
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922896
    reference: chr 2
allele count: 1
allele frequency: 8.300270588821196e-6
allele num: 120478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.560G>A
  hgvsp: ENSP00000398112.1:p.Ser187Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.512G>A
  hgvsp: ENSP00000414546.3:p.Ser171Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.512G>A
  hgvsp: ENSP00000388072.2:p.Ser171Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.512G>A
  hgvsp: ENSP00000347972.3:p.Ser171Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.512G>A
  hgvsp: ENSP00000264436.3:p.Ser171Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.512G>A
  hgvsp: ENSP00000430243.1:p.Ser171Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.512G>A
  hgvsp: ENSP00000412357.1:p.Ser171Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.512G>A
  hgvsp: ENSP00000384303.2:p.Ser171Asn
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.512G>A
  hgvsp: ENSP00000384677.2:p.Ser171Asn
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6447
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser171Asn
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

2-70922897-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922897
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922897
    reference: chr 2
allele count: 1
allele frequency: 8.302200083022e-6
allele num: 120450
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.511A>G
  hgvsp: ENSP00000384303.2:p.Ser171Gly
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.511A>G
  hgvsp: ENSP00000264436.3:p.Ser171Gly
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.511A>G
  hgvsp: ENSP00000412357.1:p.Ser171Gly
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.511A>G
  hgvsp: ENSP00000430243.1:p.Ser171Gly
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.559A>G
  hgvsp: ENSP00000398112.1:p.Ser187Gly
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.511A>G
  hgvsp: ENSP00000384677.2:p.Ser171Gly
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.511A>G
  hgvsp: ENSP00000347972.3:p.Ser171Gly
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.511A>G
  hgvsp: ENSP00000388072.2:p.Ser171Gly
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.511A>G
  hgvsp: ENSP00000414546.3:p.Ser171Gly
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser171Gly
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

2-70922898-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922898
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922898
    reference: chr 2
allele count: 1
allele frequency: 8.303992559622666e-6
allele num: 120424
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.510C>T
  hgvsp: ENST00000456320.3:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.510C>T
  hgvsp: ENST00000403045.2:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.510C>T
  hgvsp: ENST00000407644.2:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.510C>T
  hgvsp: ENST00000264436.4:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.510C>T
  hgvsp: ENST00000355733.3:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.510C>T
  hgvsp: ENST00000413157.2:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.558C>T
  hgvsp: ENST00000430656.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.510C>T
  hgvsp: ENST00000522886.1:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.510C>T
  hgvsp: ENST00000415348.1:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile170Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

2-70922908-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922908
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922908
    reference: chr 2
allele count: 2
allele frequency: 1.667139022723105e-5
allele num: 119966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.500A>G
  hgvsp: ENSP00000384677.2:p.His167Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.500A>G
  hgvsp: ENSP00000388072.2:p.His167Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.500A>G
  hgvsp: ENSP00000412357.1:p.His167Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.500A>G
  hgvsp: ENSP00000384303.2:p.His167Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.500A>G
  hgvsp: ENSP00000347972.3:p.His167Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.500A>G
  hgvsp: ENSP00000264436.3:p.His167Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.548A>G
  hgvsp: ENSP00000398112.1:p.His183Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.500A>G
  hgvsp: ENSP00000414546.3:p.His167Arg
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.500A>G
  hgvsp: ENSP00000430243.1:p.His167Arg
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2747
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His167Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD

2-70922912-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922912
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922912
    reference: chr 2
allele count: 1
allele frequency: 8.350451759440186e-6
allele num: 119754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.496G>C
  hgvsp: ENSP00000384303.2:p.Asp166His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.496G>C
  hgvsp: ENSP00000388072.2:p.Asp166His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.496G>C
  hgvsp: ENSP00000430243.1:p.Asp166His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.496G>C
  hgvsp: ENSP00000347972.3:p.Asp166His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.496G>C
  hgvsp: ENSP00000264436.3:p.Asp166His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.496G>C
  hgvsp: ENSP00000414546.3:p.Asp166His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.496G>C
  hgvsp: ENSP00000384677.2:p.Asp166His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.544G>C
  hgvsp: ENSP00000398112.1:p.Asp182His
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.496G>C
  hgvsp: ENSP00000412357.1:p.Asp166His
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1423
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp166His
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

2-70922933-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922933
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922933
    reference: chr 2
allele count: 1
allele frequency: 8.517597356137781e-6
allele num: 117404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.475T>C
  hgvsp: ENST00000415348.1:c.475T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.475T>C
  hgvsp: ENST00000264436.4:c.475T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.475T>C
  hgvsp: ENST00000456320.3:c.475T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.475T>C
  hgvsp: ENST00000522886.1:c.475T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.523T>C
  hgvsp: ENST00000430656.1:c.523T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.475T>C
  hgvsp: ENST00000355733.3:c.475T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.475T>C
  hgvsp: ENST00000407644.2:c.475T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.475T>C
  hgvsp: ENST00000403045.2:c.475T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.475T>C
  hgvsp: ENST00000413157.2:c.475T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: c.475T>C
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-70922934-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922934
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922934
    reference: chr 2
allele count: 1
allele frequency: 8.518177791406862e-6
allele num: 117396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.475-1G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.475-1G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.475-1G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.475-1G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.475-1G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.475-1G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.523-1G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.475-1G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.475-1G>A
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4269
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: c.475-1G>A
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

2-70922937-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922937
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922937
    reference: chr 2
allele count: 1
allele frequency: 8.557540905045526e-6
allele num: 116856
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.475-4C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.475-4C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.523-4C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.475-4C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.475-4C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.475-4C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.475-4C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.475-4C>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.475-4C>A
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39496
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
hgvs: c.475-4C>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

2-70922959-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922959
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922959
    reference: chr 2
allele count: 4
allele frequency: 3.603798403517307e-5
allele num: 110994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.475-26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.475-26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.523-26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.475-26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.475-26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.475-26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.475-26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.475-26C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.475-26C>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18070
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19507
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3200
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4465
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14394
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2741
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD

2-70922961-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922961
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922961
    reference: chr 2
allele count: 1
allele frequency: 9.030650026188885e-6
allele num: 110734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.475-28C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.475-28C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.475-28C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.523-28C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.475-28C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.475-28C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.475-28C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.475-28C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.475-28C>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4445
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3255
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3120
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

2-70922962-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922962
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922962
    reference: chr 2
allele count: 15
allele frequency: 1.358720266671498e-4
allele num: 110398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.475-29G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.475-29G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.523-29G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.475-29G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.475-29G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.475-29G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.475-29G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.475-29G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.475-29G>A
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18797
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11858
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3630
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6266
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4672
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

2-70922985-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70922985
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70922985
    reference: chr 2
allele count: 35
allele frequency: 3.547249361495115e-4
allele num: 98668
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.475-52G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.475-52G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.475-52G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.523-52G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.475-52G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.475-52G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.475-52G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.475-52G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.475-52G>C
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14659
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 18103
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8584
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7986
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4706
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

2-70923329-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923329
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923329
    reference: chr 2
allele count: 1
allele frequency: 1.361025668944116e-5
allele num: 73474
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+48C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+48C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+48C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+48C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+48C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+48C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+48C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+48C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+48C>G
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19073
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7211
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5822
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5341
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7978
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

2-70923334-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923334
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923334
    reference: chr 2
allele count: 2
allele frequency: 2.701972439881113e-5
allele num: 74020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+43T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+43T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+43T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+43T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+43T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+43T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+43T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+43T>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+43T>C
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1885
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2607
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5857
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7900
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

2-70923338-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923338
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923338
    reference: chr 2
allele count: 2
allele frequency: 2.684059371393295e-5
allele num: 74514
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+39G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+39G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+39G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+39G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+39G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+39G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+39G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+39G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+39G>A
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19043
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19999
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2501
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5895
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2327
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

2-70923339-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923339
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923339
    reference: chr 2
allele count: 2
allele frequency: 2.674511901577962e-5
allele num: 74780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+38T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+38T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+38T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+38T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+38T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+38T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+38T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+38T>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+38T>A
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20075
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18927
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18895
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1599
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2432
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

2-70923340-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923340
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923340
    reference: chr 2
allele count: 3
allele frequency: 4.008230232744569e-5
allele num: 74846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+37A>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+37A>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+37A>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+37A>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+37A>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+37A>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+37A>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+37A>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+37A>C
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18898
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20109
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4887
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7788
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2366
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1527
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-70923345-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923345
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923345
    reference: chr 2
allele count: 1
allele frequency: 1.321702352630188e-5
allele num: 75660
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+32A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+32A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+32A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+32A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+32A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+32A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+32A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+32A>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+32A>G
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7684
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7547
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7825
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4686
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

2-70923350-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923350
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923350
    reference: chr 2
allele count: 4
allele frequency: 5.217845030002609e-5
allele num: 76660
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+27G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+27G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+27G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+27G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+27G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+27G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+27G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+27G>C
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+27G>C
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17557
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19930
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5671
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1848
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/2-70923352-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923352
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923352
    reference: chr 2
allele count: 1
allele frequency: 1.291722641314457e-5
allele num: 77416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+25G>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+25G>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+25G>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+25G>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+25G>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+25G>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+25G>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+25G>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+25G>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19860
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1666
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1961
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10356
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6982
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/2-70923354-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923354
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923353
    reference: chr 2
allele count: 1
allele frequency: 1.282873636946761e-5
allele num: 77950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+22delT
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+22delT
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+22delT
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+22delT
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+22delT
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+22delT
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+22delT
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+22delT
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+22delT
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10728
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11031
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: CA
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

2-70923363-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923363
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923363
    reference: chr 2
allele count: 1
allele frequency: 1.230890426134266e-5
allele num: 81242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+14C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+14C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+14C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+14C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+14C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+14C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+14C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+14C>G
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+14C>G
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14077
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4854
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19711
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3050
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14878
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

2-70923364-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923364
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923364
    reference: chr 2
allele count: 20
allele frequency: 2.448639780601876e-4
allele num: 81678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+13C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+13C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+13C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+13C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+13C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+13C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+13C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+13C>T
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+13C>T
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13858
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15018
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18636
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2252
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1918
  bin: 9.75e1
  variant carriers: 22
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

2-70923365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 70923365
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 70923365
    reference: chr 2
allele count: 10
allele frequency: 1.219898992363432e-4
allele num: 81974
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000264436
  ensembl transcript: ENST00000264436
  gene symbol: ADD2
  hgvsc: ENST00000264436.4:c.474+12G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000412357
  ensembl transcript: ENST00000415348
  gene symbol: ADD2
  hgvsc: ENST00000415348.1:c.474+12G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000398112
  ensembl transcript: ENST00000430656
  gene symbol: ADD2
  hgvsc: ENST00000430656.1:c.522+12G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384303
  ensembl transcript: ENST00000403045
  gene symbol: ADD2
  hgvsc: ENST00000403045.2:c.474+12G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000430243
  ensembl transcript: ENST00000522886
  gene symbol: ADD2
  hgvsc: ENST00000522886.1:c.474+12G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000384677
  ensembl transcript: ENST00000407644
  gene symbol: ADD2
  hgvsc: ENST00000407644.2:c.474+12G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000347972
  ensembl transcript: ENST00000355733
  gene symbol: ADD2
  hgvsc: ENST00000355733.3:c.474+12G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000388072
  ensembl transcript: ENST00000413157
  gene symbol: ADD2
  hgvsc: ENST00000413157.2:c.474+12G>A
  variant of: http://identifiers.org/hgnc/244
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000075340
  ensembl protein: ENSP00000414546
  ensembl transcript: ENST00000456320
  gene symbol: ADD2
  hgvsc: ENST00000456320.3:c.474+12G>A
  variant of: http://identifiers.org/hgnc/244
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18422
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15429
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13626
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 357
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 200
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1762
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5088
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5876
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.856100926473487e-5
allele num: 10146
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.610108303249097e-4
allele num: 11080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63040
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.72e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.166e-1

DP
type: SiteQuality
SIO_000300: 1.343174e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

QD
type: SiteQuality
SIO_000300: 8.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

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

GenotypeQuality
all individuals: 1603
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 15

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5968
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63668
num of homozygotes: 0

Latino
type: Population
allele count: 16
allele frequency: 1.433434868303171e-3
allele num: 11162
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.964e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

QD
type: SiteQuality
SIO_000300: 1.279e1

FS
type: SiteQuality
SIO_000300: 5.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.355808e6

GenotypeQuality
all individuals: 349
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5060
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561231499406732e-5
allele num: 64052
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

FS
type: SiteQuality
SIO_000300: 1.4876e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.215e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.78e-1

DP
type: SiteQuality
SIO_000300: 1.370119e6

QD
type: SiteQuality
SIO_000300: 8.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1104
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1581
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2220
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5026
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 348
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.909479686386316e-5
allele num: 11224
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9982
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.379923e6

QD
type: SiteQuality
SIO_000300: 1.61e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

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

GenotypeQuality
all individuals: 1462
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32994
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
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variant carriers: 0

GenotypeQuality
all individuals: 5093
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2020
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1822
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1508
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.657951122566221e-5
allele num: 64406
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6056
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.349e1

DP
type: SiteQuality
SIO_000300: 1.383864e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

FS
type: SiteQuality
SIO_000300: 2.888e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
all individuals: 747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33827
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1497
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 1854
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
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variant carriers: 0

GenotypeQuality
all individuals: 2081
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.408504963698325e-5
allele num: 13498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.901548869503294e-5
allele num: 11234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6054
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.287e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.871e0

QD
type: SiteQuality
SIO_000300: 1.634e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 5.274e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e-1

DP
type: SiteQuality
SIO_000300: 1.391016e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.83e-1

GenotypeQuality
all individuals: 5195
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 754
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 34898
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.089948397861756e-5
allele num: 64726
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11262
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.1697e1

MQRankSum
type: SiteQuality
SIO_000300: -6.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e0

VQSLOD
type: SiteQuality
SIO_000300: -1.293e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.395472e6

QD
type: SiteQuality
SIO_000300: 1.28e1

GenotypeQuality
all individuals: 760
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1913
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1443
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 291
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variant carriers: 0

GenotypeQuality
all individuals: 4026
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.869966294128082e-5
allele num: 11274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14310
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.406099e6

MQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

QD
type: SiteQuality
SIO_000300: 2.256e1

VQSLOD
type: SiteQuality
SIO_000300: -1.524e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.886e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.31e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.082139004469102e-5
allele num: 64890
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6126
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.26e-1

FS
type: SiteQuality
SIO_000300: 2.226e0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e-1

DP
type: SiteQuality
SIO_000300: 1.41108e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 1.203e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14676
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.050910789350771e-3
allele num: 8564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11306
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.639e0

DP
type: SiteQuality
SIO_000300: 1.417555e6

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.218e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: -4.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e-2

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.844861135680169e-5
allele num: 11306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14676
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: -4.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.639e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.417555e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e-2

QD
type: SiteQuality
SIO_000300: 1.218e1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6194
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.984126984126984e-4
allele num: 10080
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65212
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.705e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.85e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

FS
type: SiteQuality
SIO_000300: 1.319e0

VQSLOD
type: SiteQuality
SIO_000300: 2.07e-1

DP
type: SiteQuality
SIO_000300: 1.42274e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.891e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 293
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11334
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.98373338623289e-4
allele num: 10082
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6220
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.907e0

QD
type: SiteQuality
SIO_000300: 1.123e1

VQSLOD
type: SiteQuality
SIO_000300: 6.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-2

DP
type: SiteQuality
SIO_000300: 1.428354e6

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.653920337997122e-5
allele num: 65326
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6254
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 1.435992e6

QD
type: SiteQuality
SIO_000300: 1.257e1

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

Latino
type: Population
allele count: 1
allele frequency: 8.818342151675486e-5
allele num: 11340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.06044376434583e-5
allele num: 65350
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6256
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.12e-1

FS
type: SiteQuality
SIO_000300: 3.052e0

DP
type: SiteQuality
SIO_000300: 1.439753e6

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.285e1

MQ
type: SiteQuality
SIO_000300: 5.922e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.65e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1052
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.512960791976033e-5
allele num: 15354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65538
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 874
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

QD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.1e-3

FS
type: SiteQuality
SIO_000300: 1.263e0

GenotypeQuality
all individuals: 5686
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

South Asian
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allele frequency: 5.192782032974166e-4
allele num: 15406
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African
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allele frequency: 1.966181675186787e-4
allele num: 10172
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65590
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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DP
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SIO_000300: 1.457184e6

ReadPosRankSum
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MQ
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InbreedingCoeff
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FS
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SIO_000300: 5.3e-1

QD
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MQRankSum
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BaseQRankSum
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SIO_000300: -2.267e0

VQSLOD
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SIO_000300: 1.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11388
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African
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allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.568381430363864e-4
allele num: 6376
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.523832744118006e-5
allele num: 65624
num of homozygotes: 0

MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

InbreedingCoeff
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SIO_000300: 1.6e-3

BaseQRankSum
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SIO_000300: 1.08e0

ClippingRankSum
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DP
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FS
type: SiteQuality
SIO_000300: 5.032e0

VQSLOD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: -2.58e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65710
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15332
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.761811792268645e-5
allele num: 10244
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.146e0

VQSLOD
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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DP
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BaseQRankSum
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MQ
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ClippingRankSum
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SIO_000300: -4.0e-3

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65682
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6454
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African
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allele count: 1
allele frequency: 9.731413001167769e-5
allele num: 10276
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15138
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 8.93e-1

FS
type: SiteQuality
SIO_000300: 1.2395e1

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-2

QD
type: SiteQuality
SIO_000300: 1.233e1

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: -2.685e0

DP
type: SiteQuality
SIO_000300: 1.481812e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.514e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.577e0

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

European (Non-Finnish)
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allele frequency: 1.536806516059628e-5
allele num: 65070
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele count: 0
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MQRankSum
type: SiteQuality
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MQ
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FS
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
type: Population
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allele frequency: 0.0e0
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African
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allele frequency: 9.832841691248771e-5
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele num: 64772
num of homozygotes: 0

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

Latino
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East Asian
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European (Non-Finnish)
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allele count: 1
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
type: Population
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South Asian
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allele num: 12134
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ClippingRankSum
type: SiteQuality
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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DP
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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South Asian
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East Asian
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Other
type: Population
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African
type: Population
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European (Non-Finnish)
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allele num: 64384
num of homozygotes: 0

MQ
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 1472
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11946
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555161581288296e-5
allele num: 64302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.933e0

VQSLOD
type: SiteQuality
SIO_000300: -2.471e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 5.583e1

FS
type: SiteQuality
SIO_000300: 1.202e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.538e0

QD
type: SiteQuality
SIO_000300: 9.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 1.421833e6

GenotypeQuality
all individuals: 1075
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 41

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.954210631096954e-5
allele num: 10046
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 42
allele frequency: 6.583691256230994e-4
allele num: 63794
num of homozygotes: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

QD
type: SiteQuality
SIO_000300: 1.359e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.38e0

DP
type: SiteQuality
SIO_000300: 1.386549e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-2

GenotypeQuality
all individuals: 5065
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10010
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.572228161750833e-5
allele num: 63604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

QD
type: SiteQuality
SIO_000300: 1.188e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.48e-1

DP
type: SiteQuality
SIO_000300: 1.369572e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.57e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1365
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1392
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variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.033423667570009e-5
allele num: 11070
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10004
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.358687e6

FS
type: SiteQuality
SIO_000300: 2.038e0

VQSLOD
type: SiteQuality
SIO_000300: 2.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.614e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 299
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 342
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 8.25e1
variant carriers: 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: 11348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.07605736068252e-5
allele num: 11018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63464
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.755e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

QD
type: SiteQuality
SIO_000300: 9.789999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.351539e6

VQSLOD
type: SiteQuality
SIO_000300: 7.49e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2074
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 280
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.395783421178726e-4
allele num: 8348
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.843296781039972e-5
allele num: 11308
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9868
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.012e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e-1

DP
type: SiteQuality
SIO_000300: 1.260782e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.27e-1

FS
type: SiteQuality
SIO_000300: 1.591e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.198178768272226e-4
allele num: 8346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62694
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.416e0

QD
type: SiteQuality
SIO_000300: 5.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.976e-1

DP
type: SiteQuality
SIO_000300: 1.25017e6

MQRankSum
type: SiteQuality
SIO_000300: 1.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 164

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8256
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.451566951566952e-4
allele num: 11232
num of homozygotes: 0

African
type: Population
allele count: 132
allele frequency: 1.356907894736842e-2
allele num: 9728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.613892385655725e-5
allele num: 61962
num of homozygotes: 0

South Asian
type: Population
allele count: 31
allele frequency: 3.365906623235613e-3
allele num: 9210
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.298701298701299e-3
allele num: 770
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.343e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e-1

DP
type: SiteQuality
SIO_000300: 1.214908e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.22e0

FS
type: SiteQuality
SIO_000300: 7.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1327
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GenotypeQuality
all individuals: 3533
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.226639132679401e-5
allele num: 61984
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11232
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8246
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.379e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.153e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.38e-1

QD
type: SiteQuality
SIO_000300: 7.63e0

DP
type: SiteQuality
SIO_000300: 1.212218e6

FS
type: SiteQuality
SIO_000300: 2.239e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 616
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 55

GenotypeQuality
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1017
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8770
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.340482573726542e-3
allele num: 746
num of homozygotes: 0

African
type: Population
allele count: 23
allele frequency: 2.426160337552743e-3
allele num: 9480
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.353057910878586e-3
allele num: 11086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 3.110368987984154e-4
allele num: 61086
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6228
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.619e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.369e0

DP
type: SiteQuality
SIO_000300: 1.198133e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.191e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2478
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11186
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.859988168014199e-5
allele num: 10142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65550
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.106e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.805e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.903e1

MQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.495113e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

GenotypeQuality
all individuals: 5985
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 29

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 511
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variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
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: 0
allele frequency: 0.0e0
allele num: 15680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

Latino
type: Population
allele count: 29
allele frequency: 2.582368655387355e-3
allele num: 11230
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.54e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

DP
type: SiteQuality
SIO_000300: 1.521153e6

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

GenotypeQuality
all individuals: 1459
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 80

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1525
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variant carriers: 0

GenotypeQuality
all individuals: 41347
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.068881808526779e-5
allele num: 65910
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.873114463176575e-5
allele num: 11270
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

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

South Asian
type: Population
allele count: 77
allele frequency: 4.887027164254887e-3
allele num: 15756
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

DP
type: SiteQuality
SIO_000300: 1.552555e6

QD
type: SiteQuality
SIO_000300: 1.218e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.506e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

GenotypeQuality
all individuals: 6332
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
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variant carriers: 0

GenotypeQuality
all individuals: 17
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2760
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 194
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15844
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.608e0

VQSLOD
type: SiteQuality
SIO_000300: 9.74e-1

QD
type: SiteQuality
SIO_000300: 1.034e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.889e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.569067e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 102
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GenotypeQuality
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GenotypeQuality
all individuals: 1458
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 128
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GenotypeQuality
all individuals: 3062
bin: 9.75e1
variant carriers: 322

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31535077564251e-4
allele num: 8638
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.116071428571429e-3
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 328
allele frequency: 2.033730158730159e-2
allele num: 16128
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66474
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.85e0

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

FS
type: SiteQuality
SIO_000300: 1.199e0

VQSLOD
type: SiteQuality
SIO_000300: 4.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.35e-2

DP
type: SiteQuality
SIO_000300: 1.601654e6

QD
type: SiteQuality
SIO_000300: 1.286e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 509
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504302304591131e-5
allele num: 66476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16120
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 3.125e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.771e0

VQSLOD
type: SiteQuality
SIO_000300: -2.562e0

MQRankSum
type: SiteQuality
SIO_000300: -1.75e-1

FS
type: SiteQuality
SIO_000300: 7.278e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-2

DP
type: SiteQuality
SIO_000300: 1.596175e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 161
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 109
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GenotypeQuality
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GenotypeQuality
all individuals: 145
bin: 2.75e1
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GenotypeQuality
all individuals: 2761
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GenotypeQuality
all individuals: 64
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GenotypeQuality
all individuals: 178
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 1579
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.654284597106506e-4
allele num: 66494
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.858045336306206e-4
allele num: 16146
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.53e-1

FS
type: SiteQuality
SIO_000300: 1.122e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.320000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

DP
type: SiteQuality
SIO_000300: 1.598594e6

QD
type: SiteQuality
SIO_000300: 1.152e1

VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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African
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Other
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ClippingRankSum
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FS
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ReadPosRankSum
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DP
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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Other
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African
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Latino
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European (Non-Finnish)
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FS
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DP
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InbreedingCoeff
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QD
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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African
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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FS
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MQ
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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South Asian
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ClippingRankSum
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MQ
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FS
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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South Asian
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Other
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QD
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FS
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ReadPosRankSum
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MQ
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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Latino
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East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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East Asian
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African
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Latino
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European (Non-Finnish)
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MQRankSum
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DP
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InbreedingCoeff
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QD
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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East Asian
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African
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Other
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South Asian
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European (Non-Finnish)
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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SIO_000300: -4.751e0

QD
type: SiteQuality
SIO_000300: 1.489e1

DP
type: SiteQuality
SIO_000300: 1.600138e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
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GenotypeQuality
all individuals: 44573
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.017319413433106e-5
allele num: 66284
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15960
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.236e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 1.593127e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 4.129e0

QD
type: SiteQuality
SIO_000300: 1.194e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15920
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.136363636363636e-3
allele num: 880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66198
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.205e1

DP
type: SiteQuality
SIO_000300: 1.589209e6

FS
type: SiteQuality
SIO_000300: 3.282e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65088
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11072
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.459113809585325e-5
allele num: 15482
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.96e0

DP
type: SiteQuality
SIO_000300: 1.540202e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.01e-1

QD
type: SiteQuality
SIO_000300: 8.380000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

FS
type: SiteQuality
SIO_000300: 1.372e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.463288521199587e-5
allele num: 15472
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65096
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.452e1

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 1.540458e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

FS
type: SiteQuality
SIO_000300: 1.361e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542305438168975e-5
allele num: 64838
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15392
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

QD
type: SiteQuality
SIO_000300: 1.486e1

FS
type: SiteQuality
SIO_000300: 7.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-1

DP
type: SiteQuality
SIO_000300: 1.528367e6

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.565e0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61714
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.996252810392206e-4
allele num: 8006
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.271448e6

MQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.6e-2

MQ
type: SiteQuality
SIO_000300: 5.92e1

FS
type: SiteQuality
SIO_000300: 9.055999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

QD
type: SiteQuality
SIO_000300: 1.388e1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.623745656480369e-5
allele num: 61586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7984
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6032
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14574
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQRankSum
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e0

MQ
type: SiteQuality
SIO_000300: 5.849e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.885155604516663e-5
allele num: 14524
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.832841691248771e-5
allele num: 10170
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 13
allele frequency: 1.362683438155136e-3
allele num: 9540
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.250933e6

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.359e1

GenotypeQuality
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variant carriers: 35

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2951
bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 2

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8737
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8852
num of homozygotes: 0

East Asian
type: Population
allele count: 31
allele frequency: 4.368658399098084e-3
allele num: 7096
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12968
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.700352526439483e-4
allele num: 8510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55148
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.186e0

QD
type: SiteQuality
SIO_000300: 1.395e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.97e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.101153e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

GenotypeQuality
all individuals: 1883
bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.489915840844579e-5
allele num: 40162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5102
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.89e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.977e0

DP
type: SiteQuality
SIO_000300: 8.34374e5

ClippingRankSum
type: SiteQuality
SIO_000300: 9.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11282
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.936565137976995e-5
allele num: 40514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5158
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.918e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 8.45328e5

FS
type: SiteQuality
SIO_000300: 9.031000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 1.545e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.513e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.901960784313725e-5
allele num: 40800
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.694e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.133e0

VQSLOD
type: SiteQuality
SIO_000300: -6.637999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

DP
type: SiteQuality
SIO_000300: 8.58476e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.217e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1573
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6682
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.884720593982025e-5
allele num: 40944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.133e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.5e-1

DP
type: SiteQuality
SIO_000300: 8.63018e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.64e-1

QD
type: SiteQuality
SIO_000300: 1.65e1

GenotypeQuality
all individuals: 5001
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 414
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variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40960
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 5.751533742331289e-4
allele num: 5216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

FS
type: SiteQuality
SIO_000300: 6.218e0

QD
type: SiteQuality
SIO_000300: 7.49e0

DP
type: SiteQuality
SIO_000300: 8.65787e5

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.477978125923736e-4
allele num: 6766
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6698
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5322
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.266e0

MQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.84117e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

QD
type: SiteQuality
SIO_000300: 5.94e0

GenotypeQuality
all individuals: 4341
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 19792
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5414
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6782
num of homozygotes: 0

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

Latino
type: Population
allele count: 4
allele frequency: 5.827505827505828e-4
allele num: 6864
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.96e0

DP
type: SiteQuality
SIO_000300: 9.08181e5

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.018e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

QD
type: SiteQuality
SIO_000300: 1.322e1

GenotypeQuality
all individuals: 786
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variant carriers: 0

GenotypeQuality
all individuals: 1080
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 168
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1003
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GenotypeQuality
all individuals: 714
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6944
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.62663906142167e-5
allele num: 11592
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42452
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.97e-1

DP
type: SiteQuality
SIO_000300: 9.2039e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.187e0

QD
type: SiteQuality
SIO_000300: 1.502e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.557e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 20158
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5441
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6759
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1005
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3849
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.799856011519078e-4
allele num: 5556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6996
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3572
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.61e0

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

DP
type: SiteQuality
SIO_000300: 9.32705e5

FS
type: SiteQuality
SIO_000300: 1.536e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.031e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 114
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1898
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5719
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 879
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.698946653075094e-4
allele num: 5886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7088
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44674
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

QD
type: SiteQuality
SIO_000300: 1.378e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 5.787e1

VQSLOD
type: SiteQuality
SIO_000300: -2.474e0

FS
type: SiteQuality
SIO_000300: 3.09e0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.246e0

DP
type: SiteQuality
SIO_000300: 9.86597e5

GenotypeQuality
all individuals: 388
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 974
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5634
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4776
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19589
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15167
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 20
allele frequency: 3.374957813027337e-3
allele num: 5926
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7108
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11906
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44940
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.9171e5

QD
type: SiteQuality
SIO_000300: 1.028e1

VQSLOD
type: SiteQuality
SIO_000300: 2.35e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 6.899999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.582e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1