21-47954489-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954489
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954489
    reference: chr 21
allele count: 1
allele frequency: 8.834390515398343e-6
allele num: 113194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.866-9A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1540-9A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1528-9A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1540-9A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1543-9A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1411-9A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1348-9A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1540-9A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.933-9A>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9495
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

21-47954504-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954504
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954504
    reference: chr 21
allele count: 1
allele frequency: 8.475007203756124e-6
allele num: 117994
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1534A>G
  hgvsp: ENSP00000383133.1:p.Thr512Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1546A>G
  hgvsp: ENSP00000392066.2:p.Thr516Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.872A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1354A>G
  hgvsp: ENSP00000400528.2:p.Thr452Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1549A>G
  hgvsp: ENSP00000323633.7:p.Thr517Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1417A>G
  hgvsp: ENSP00000430249.1:p.Thr473Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.939A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1546A>G
  hgvsp: ENSP00000393434.3:p.Thr516Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1546A>G
  hgvsp: ENSP00000415089.3:p.Thr516Ala
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3745
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr516Ala
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/21-47954506-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954506
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954506
    reference: chr 21
allele count: 1
allele frequency: 8.45508658008658e-6
allele num: 118272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1356C>A
  hgvsp: ENST00000427143.2:c.1356C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1548C>A
  hgvsp: ENST00000435722.3:c.1548C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.941C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1419C>A
  hgvsp: ENST00000466639.1:c.1419C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.874C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1548C>A
  hgvsp: ENST00000457905.3:c.1548C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1551C>A
  hgvsp: ENST00000318711.7:c.1551C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1536C>A
  hgvsp: ENST00000400274.1:c.1536C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1548C>A
  hgvsp: ENST00000417564.2:c.1548C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44239
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr516Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

21-47954522-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954522
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954522
    reference: chr 21
allele count: 2
allele frequency: 1.677458315160868e-5
allele num: 119228
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1564A>G
  hgvsp: ENSP00000392066.2:p.Thr522Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1567A>G
  hgvsp: ENSP00000323633.7:p.Thr523Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1552A>G
  hgvsp: ENSP00000383133.1:p.Thr518Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.890A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1435A>G
  hgvsp: ENSP00000430249.1:p.Thr479Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1564A>G
  hgvsp: ENSP00000393434.3:p.Thr522Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1564A>G
  hgvsp: ENSP00000415089.3:p.Thr522Ala
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.957A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1372A>G
  hgvsp: ENSP00000400528.2:p.Thr458Ala
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11369
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr522Ala
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

21-47954524-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954524
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954524
    reference: chr 21
allele count: 1
allele frequency: 8.387010198604401e-6
allele num: 119232
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1566G>A
  hgvsp: ENST00000417564.2:c.1566G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1566G>A
  hgvsp: ENST00000457905.3:c.1566G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1374G>A
  hgvsp: ENST00000427143.2:c.1374G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1569G>A
  hgvsp: ENST00000318711.7:c.1569G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1554G>A
  hgvsp: ENST00000400274.1:c.1554G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1566G>A
  hgvsp: ENST00000435722.3:c.1566G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1437G>A
  hgvsp: ENST00000466639.1:c.1437G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.959G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.892G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr522Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

21-47954536-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954536
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954536
    reference: chr 21
allele count: 3
allele frequency: 2.515892051458379e-5
allele num: 119242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1449A>G
  hgvsp: ENST00000466639.1:c.1449A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1578A>G
  hgvsp: ENST00000417564.2:c.1578A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1578A>G
  hgvsp: ENST00000435722.3:c.1578A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1581A>G
  hgvsp: ENST00000318711.7:c.1581A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1566A>G
  hgvsp: ENST00000400274.1:c.1566A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.904A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1578A>G
  hgvsp: ENST00000457905.3:c.1578A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.971A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1386A>G
  hgvsp: ENST00000427143.2:c.1386A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr526Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

21-47954545-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954545
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954545
    reference: chr 21
allele count: 5
allele frequency: 4.201963157187038e-5
allele num: 118992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1590C>T
  hgvsp: ENST00000318711.7:c.1590C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1458C>T
  hgvsp: ENST00000466639.1:c.1458C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1587C>T
  hgvsp: ENST00000457905.3:c.1587C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1575C>T
  hgvsp: ENST00000400274.1:c.1575C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1587C>T
  hgvsp: ENST00000435722.3:c.1587C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1587C>T
  hgvsp: ENST00000417564.2:c.1587C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1395C>T
  hgvsp: ENST00000427143.2:c.1395C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.913C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.980C>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43189
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His529His
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

21-47954563-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954563
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954563
    reference: chr 21
allele count: 1
allele frequency: 8.501377223110144e-6
allele num: 117628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1605G>A
  hgvsp: ENST00000457905.3:c.1605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1593G>A
  hgvsp: ENST00000400274.1:c.1593G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1605G>A
  hgvsp: ENST00000435722.3:c.1605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1476G>A
  hgvsp: ENST00000466639.1:c.1476G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.998G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.931G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1605G>A
  hgvsp: ENST00000417564.2:c.1605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1413G>A
  hgvsp: ENST00000427143.2:c.1413G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1608G>A
  hgvsp: ENST00000318711.7:c.1608G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln535Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

21-47954563-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954563
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954563
    reference: chr 21
allele count: 1
allele frequency: 8.501377223110144e-6
allele num: 117628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.931G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1476G>T
  hgvsp: ENSP00000430249.1:p.Gln492His
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1608G>T
  hgvsp: ENSP00000323633.7:p.Gln536His
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1413G>T
  hgvsp: ENSP00000400528.2:p.Gln471His
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1605G>T
  hgvsp: ENSP00000415089.3:p.Gln535His
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1593G>T
  hgvsp: ENSP00000383133.1:p.Gln531His
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1605G>T
  hgvsp: ENSP00000393434.3:p.Gln535His
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1605G>T
  hgvsp: ENSP00000392066.2:p.Gln535His
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.998G>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln535His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

21-47954567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954567
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954567
    reference: chr 21
allele count: 68
allele frequency: 5.821120394466511e-4
allele num: 116816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1597C>T
  hgvsp: ENSP00000383133.1:p.Arg533Trp
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1609C>T
  hgvsp: ENSP00000415089.3:p.Arg537Trp
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1002C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1480C>T
  hgvsp: ENSP00000430249.1:p.Arg494Trp
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.935C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1612C>T
  hgvsp: ENSP00000323633.7:p.Arg538Trp
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1609C>T
  hgvsp: ENSP00000393434.3:p.Arg537Trp
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1609C>T
  hgvsp: ENSP00000392066.2:p.Arg537Trp
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1417C>T
  hgvsp: ENSP00000400528.2:p.Arg473Trp
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 11791
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 40188
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3438
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg537Trp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

21-47954568-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954568
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954568
    reference: chr 21
allele count: 1
allele frequency: 8.565310492505354e-6
allele num: 116750
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1610G>A
  hgvsp: ENSP00000392066.2:p.Arg537Gln
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1481G>A
  hgvsp: ENSP00000430249.1:p.Arg494Gln
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1418G>A
  hgvsp: ENSP00000400528.2:p.Arg473Gln
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1613G>A
  hgvsp: ENSP00000323633.7:p.Arg538Gln
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1610G>A
  hgvsp: ENSP00000415089.3:p.Arg537Gln
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1598G>A
  hgvsp: ENSP00000383133.1:p.Arg533Gln
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.936G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1610G>A
  hgvsp: ENSP00000393434.3:p.Arg537Gln
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1003G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg537Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

21-47954570-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954570
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954570
    reference: chr 21
allele count: 34
allele frequency: 2.920510573966225e-4
allele num: 116418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1420G>A
  hgvsp: ENSP00000400528.2:p.Ala474Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1612G>A
  hgvsp: ENSP00000392066.2:p.Ala538Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1483G>A
  hgvsp: ENSP00000430249.1:p.Ala495Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1615G>A
  hgvsp: ENSP00000323633.7:p.Ala539Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1612G>A
  hgvsp: ENSP00000393434.3:p.Ala538Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1612G>A
  hgvsp: ENSP00000415089.3:p.Ala538Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1005G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1600G>A
  hgvsp: ENSP00000383133.1:p.Ala534Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.938G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39660
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11851
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala538Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

21-47954582-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954582
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954582
    reference: chr 21
allele count: 4
allele frequency: 3.554102322605868e-5
allele num: 112546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1627G>A
  hgvsp: ENSP00000323633.7:p.Ala543Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1612G>A
  hgvsp: ENSP00000383133.1:p.Ala538Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1624G>A
  hgvsp: ENSP00000393434.3:p.Ala542Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1495G>A
  hgvsp: ENSP00000430249.1:p.Ala499Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.950G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1017G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1624G>A
  hgvsp: ENSP00000392066.2:p.Ala542Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1624G>A
  hgvsp: ENSP00000415089.3:p.Ala542Thr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1432G>A
  hgvsp: ENSP00000400528.2:p.Ala478Thr
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35175
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala542Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

21-47954583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954583
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954583
    reference: chr 21
allele count: 5
allele frequency: 4.464126281204243e-5
allele num: 112004
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1496C>T
  hgvsp: ENSP00000430249.1:p.Ala499Val
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1625C>T
  hgvsp: ENSP00000415089.3:p.Ala542Val
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.951C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1628C>T
  hgvsp: ENSP00000323633.7:p.Ala543Val
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1433C>T
  hgvsp: ENSP00000400528.2:p.Ala478Val
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1613C>T
  hgvsp: ENSP00000383133.1:p.Ala538Val
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1625C>T
  hgvsp: ENSP00000392066.2:p.Ala542Val
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1625C>T
  hgvsp: ENSP00000393434.3:p.Ala542Val
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1018C>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8457
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala542Val
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

21-47954584-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954584
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954584
    reference: chr 21
allele count: 14
allele frequency: 1.250759389629418e-4
allele num: 111932
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1019G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1626G>A
  hgvsp: ENST00000435722.3:c.1626G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1434G>A
  hgvsp: ENST00000427143.2:c.1434G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1626G>A
  hgvsp: ENST00000457905.3:c.1626G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1614G>A
  hgvsp: ENST00000400274.1:c.1614G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1629G>A
  hgvsp: ENST00000318711.7:c.1629G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1497G>A
  hgvsp: ENST00000466639.1:c.1497G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1626G>A
  hgvsp: ENST00000417564.2:c.1626G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.952G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34590
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala542Ala
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

21-47954586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954586
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954586
    reference: chr 21
allele count: 2
allele frequency: 1.795493311787414e-5
allele num: 111390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.954G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1499G>A
  hgvsp: ENSP00000430249.1:p.Cys500Tyr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1628G>A
  hgvsp: ENSP00000392066.2:p.Cys543Tyr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1628G>A
  hgvsp: ENSP00000415089.3:p.Cys543Tyr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1436G>A
  hgvsp: ENSP00000400528.2:p.Cys479Tyr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1631G>A
  hgvsp: ENSP00000323633.7:p.Cys544Tyr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1616G>A
  hgvsp: ENSP00000383133.1:p.Cys539Tyr
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1021G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1628G>A
  hgvsp: ENSP00000393434.3:p.Cys543Tyr
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34037
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40645
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys543Tyr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

21-47954607-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954607
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954607
    reference: chr 21
allele count: 1
allele frequency: 1.017231908530507e-5
allele num: 98306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1513+7G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1645+7G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1642+7G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1642+7G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1630+7G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1035+7G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1642+7G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.968+7G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1450+7G>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15652
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3990
  bin: 2.75e1
  variant carriers: 0
hgvs: c.1642+7G>C
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

21-47954613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954613
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954613
    reference: chr 21
allele count: 5
allele frequency: 5.29829394934831e-5
allele num: 94370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1035+13G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1513+13G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1642+13G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1642+13G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1450+13G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.968+13G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1642+13G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1645+13G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1630+13G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22193
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1788
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4110
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 9.75e1
  variant carriers: 5
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ

21-47954617-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954617
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954617
    reference: chr 21
allele count: 2
allele frequency: 2.208236722976703e-5
allele num: 90570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1630+17G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1642+17G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1645+17G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1642+17G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1642+17G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1513+17G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1035+17G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.968+17G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1450+17G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24339
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5192
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

21-47954623-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954623
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954623
    reference: chr 21
allele count: 48
allele frequency: 5.49437970742428e-4
allele num: 87362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1513+23C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1630+23C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1450+23C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1035+23C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1642+23C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1645+23C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1642+23C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1642+23C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.968+23C>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24939
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13458
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7808
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 1.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 9659
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4943
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28465
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.25e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

21-47954624-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954624
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954624
    reference: chr 21
allele count: 74
allele frequency: 8.532423208191126e-4
allele num: 86728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1642+24G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1450+24G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1630+24G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1642+24G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1642+24G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1513+24G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1645+24G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.968+24G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1035+24G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25105
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7368
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6027
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 13736
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28761
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 8.75e1
  variant carriers: 3
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

21-47954628-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954628
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954628
    reference: chr 21
allele count: 1
allele frequency: 1.222224938277641e-5
allele num: 81818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1450+28G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1645+28G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.968+28G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1642+28G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1513+28G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1630+28G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1035+28G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1642+28G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1642+28G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24858
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14860
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6187
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5743
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

21-47954647-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47954647
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47954647
    reference: chr 21
allele count: 0
allele frequency: 0.0e0
allele num: 66820
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1642+47G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1450+47G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1642+47G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1642+47G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1513+47G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1035+47G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1645+47G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.968+47G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1630+47G>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19648
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21053
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7755
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5428
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4971
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

21-47957099-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957099
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957099
    reference: chr 21
allele count: 2
allele frequency: 1.656287266463495e-5
allele num: 120752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.969-38G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1451-38G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1643-38G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1514-38G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1643-38G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1036-38G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1631-38G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1643-38G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1646-38G>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50105
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

21-47957120-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957120
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957120
    reference: chr 21
allele count: 5
allele frequency: 4.140238146498186e-5
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.969-17T>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1631-17T>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1514-17T>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1643-17T>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1646-17T>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1643-17T>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1643-17T>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1036-17T>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1451-17T>G
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57571
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

21-47957134-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957134
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957134
    reference: chr 21
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1514-3C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.969-3C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1646-3C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1643-3C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1643-3C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1643-3C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1451-3C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1036-3C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1631-3C>G
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57571
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
hgvs: c.1643-3C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

21-47957135-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957135
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957135
    reference: chr 21
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.969-2A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1643-2A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1631-2A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1643-2A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1643-2A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1646-2A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1036-2A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1514-2A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1451-2A>G
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57571
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
hgvs: c.1643-2A>G
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

21-47957153-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957153
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957153
    reference: chr 21
allele count: 4
allele frequency: 3.312190517198549e-5
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1467C>T
  hgvsp: ENST00000427143.2:c.1467C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1659C>T
  hgvsp: ENST00000417564.2:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1659C>T
  hgvsp: ENST00000435722.3:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1052C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1662C>T
  hgvsp: ENST00000318711.7:c.1662C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1659C>T
  hgvsp: ENST00000457905.3:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1530C>T
  hgvsp: ENST00000466639.1:c.1530C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1647C>T
  hgvsp: ENST00000400274.1:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.985C>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50107
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn553Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

21-47957154-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957154
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957154
    reference: chr 21
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.986G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1663G>T
  hgvsp: ENSP00000323633.7:p.Val555Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1531G>T
  hgvsp: ENSP00000430249.1:p.Val511Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1660G>T
  hgvsp: ENSP00000393434.3:p.Val554Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1660G>T
  hgvsp: ENSP00000392066.2:p.Val554Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1468G>T
  hgvsp: ENSP00000400528.2:p.Val490Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1648G>T
  hgvsp: ENSP00000383133.1:p.Val550Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1053G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1660G>T
  hgvsp: ENSP00000415089.3:p.Val554Leu
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val554Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

21-47957189-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957189
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957189
    reference: chr 21
allele count: 2
allele frequency: 1.656012983141788e-5
allele num: 120772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1695T>C
  hgvsp: ENST00000435722.3:c.1695T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1088T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1566T>C
  hgvsp: ENST00000466639.1:c.1566T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1698T>C
  hgvsp: ENST00000318711.7:c.1698T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1695T>C
  hgvsp: ENST00000417564.2:c.1695T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1683T>C
  hgvsp: ENST00000400274.1:c.1683T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1021T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1695T>C
  hgvsp: ENST00000457905.3:c.1695T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1503T>C
  hgvsp: ENST00000427143.2:c.1503T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His565His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

21-47957192-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957192
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957192
    reference: chr 21
allele count: 4
allele frequency: 3.312025966283576e-5
allele num: 120772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1698C>T
  hgvsp: ENST00000435722.3:c.1698C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1024C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1698C>T
  hgvsp: ENST00000457905.3:c.1698C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1686C>T
  hgvsp: ENST00000400274.1:c.1686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1698C>T
  hgvsp: ENST00000417564.2:c.1698C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1091C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1701C>T
  hgvsp: ENST00000318711.7:c.1701C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1569C>T
  hgvsp: ENST00000466639.1:c.1569C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1506C>T
  hgvsp: ENST00000427143.2:c.1506C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57571
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly566Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

21-47957192-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957192
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957192
    reference: chr 21
allele count: 1
allele frequency: 8.280064915708939e-6
allele num: 120772
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1698C>G
  hgvsp: ENST00000457905.3:c.1698C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1506C>G
  hgvsp: ENST00000427143.2:c.1506C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1698C>G
  hgvsp: ENST00000435722.3:c.1698C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1091C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1024C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1686C>G
  hgvsp: ENST00000400274.1:c.1686C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1701C>G
  hgvsp: ENST00000318711.7:c.1701C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1698C>G
  hgvsp: ENST00000417564.2:c.1698C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1569C>G
  hgvsp: ENST00000466639.1:c.1569C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly566Gly
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

21-47957193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957193
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957193
    reference: chr 21
allele count: 6
allele frequency: 4.968038949425363e-5
allele num: 120772
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1699G>A
  hgvsp: ENSP00000392066.2:p.Val567Met
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1507G>A
  hgvsp: ENSP00000400528.2:p.Val503Met
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1092G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1570G>A
  hgvsp: ENSP00000430249.1:p.Val524Met
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1687G>A
  hgvsp: ENSP00000383133.1:p.Val563Met
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1702G>A
  hgvsp: ENSP00000323633.7:p.Val568Met
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1699G>A
  hgvsp: ENSP00000415089.3:p.Val567Met
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1699G>A
  hgvsp: ENSP00000393434.3:p.Val567Met
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1025G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val567Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

21-47957193-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957193
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957193
    reference: chr 21
allele count: 1
allele frequency: 8.280064915708939e-6
allele num: 120772
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1699G>C
  hgvsp: ENSP00000392066.2:p.Val567Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1092G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1702G>C
  hgvsp: ENSP00000323633.7:p.Val568Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1699G>C
  hgvsp: ENSP00000393434.3:p.Val567Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1570G>C
  hgvsp: ENSP00000430249.1:p.Val524Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1687G>C
  hgvsp: ENSP00000383133.1:p.Val563Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1699G>C
  hgvsp: ENSP00000415089.3:p.Val567Leu
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1025G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1507G>C
  hgvsp: ENSP00000400528.2:p.Val503Leu
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val567Leu
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

21-47957195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957195
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957195
    reference: chr 21
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1572G>A
  hgvsp: ENST00000466639.1:c.1572G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1509G>A
  hgvsp: ENST00000427143.2:c.1509G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1689G>A
  hgvsp: ENST00000400274.1:c.1689G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1704G>A
  hgvsp: ENST00000318711.7:c.1704G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1027G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1701G>A
  hgvsp: ENST00000435722.3:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1701G>A
  hgvsp: ENST00000417564.2:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1701G>A
  hgvsp: ENST00000457905.3:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1094G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val567Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS

21-47957196-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957196
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957196
    reference: chr 21
allele count: 1
allele frequency: 8.280064915708939e-6
allele num: 120772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1573T>C
  hgvsp: ENST00000466639.1:c.1573T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1095T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1028T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1705T>C
  hgvsp: ENST00000318711.7:c.1705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1702T>C
  hgvsp: ENST00000435722.3:c.1702T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1690T>C
  hgvsp: ENST00000400274.1:c.1690T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1702T>C
  hgvsp: ENST00000457905.3:c.1702T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1702T>C
  hgvsp: ENST00000417564.2:c.1702T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1510T>C
  hgvsp: ENST00000427143.2:c.1510T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu568Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

21-47957201-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957201
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957201
    reference: chr 21
allele count: 2
allele frequency: 1.656012983141788e-5
allele num: 120772
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1033A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1100A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1710A>G
  hgvsp: ENST00000318711.7:c.1710A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1707A>G
  hgvsp: ENST00000435722.3:c.1707A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1578A>G
  hgvsp: ENST00000466639.1:c.1578A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1707A>G
  hgvsp: ENST00000417564.2:c.1707A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1707A>G
  hgvsp: ENST00000457905.3:c.1707A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1695A>G
  hgvsp: ENST00000400274.1:c.1695A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1515A>G
  hgvsp: ENST00000427143.2:c.1515A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1707A>G
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

21-47957202-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957202
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957202
    reference: chr 21
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1710+1G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1578+1G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1515+1G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1707+1G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1033+1G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1695+1G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1100+1G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1707+1G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1707+1G>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
hgvs: c.1707+1G>C
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

21-47957204-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957204
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957204
    reference: chr 21
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1710+3G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1707+3G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1578+3G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1707+3G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1707+3G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1515+3G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1695+3G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1033+3G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1100+3G>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1707+3G>C
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

21-47957208-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957208
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957208
    reference: chr 21
allele count: 15
allele frequency: 1.241989169854439e-4
allele num: 120774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1100+7G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1707+7G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1707+7G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1695+7G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1707+7G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1515+7G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1710+7G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1578+7G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1033+7G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1707+7G>A
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

21-47957211-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957211
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957211
    reference: chr 21
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1695+10G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1710+10G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1515+10G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1707+10G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1707+10G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1578+10G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1707+10G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1033+10G>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1100+10G>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

21-47957230-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957230
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957230
    reference: chr 21
allele count: 1
allele frequency: 8.279790686891435e-6
allele num: 120776
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1710+29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1515+29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1033+29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1695+29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1707+29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1100+29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1707+29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1578+29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1707+29T>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50106
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/21-47957236-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957236
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957236
    reference: chr 21
allele count: 8
allele frequency: 6.623832549513148e-5
allele num: 120776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1033+35C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1710+35C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1100+35C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1578+35C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1707+35C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1707+35C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1695+35C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1707+35C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1515+35C>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50111
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

21-47957236-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957236
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957236
    reference: chr 21
allele count: 162
allele frequency: 1.341326091276413e-3
allele num: 120776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1515+35C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1707+35C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1578+35C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1100+35C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1710+35C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1707+35C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1707+35C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1033+35C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1695+35C>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50111
  bin: 9.75e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

21-47957238-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957238
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957238
    reference: chr 21
allele count: 3
allele frequency: 2.483854942871336e-5
allele num: 120780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1033+37A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1578+37A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1100+37A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1707+37A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1707+37A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1710+37A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1707+37A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1695+37A>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1515+37A>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50110
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

21-47957321-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957321
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957321
    reference: chr 21
allele count: 3
allele frequency: 2.536097115612214e-5
allele num: 118292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-38C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-38C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-38C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-38C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-38C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-38C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-38C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-38C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-38C>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4202
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14877
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2224
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39863
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

21-47957321-CGGG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957321
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957318
    reference: chr 21
allele count: 1
allele frequency: 8.453657052040712e-6
allele num: 118292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-37_1101-35delGGG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-37_1711-35delGGG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-37_1708-35delGGG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-37_1708-35delGGG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-37_1579-35delGGG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-37_1516-35delGGG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-37_1708-35delGGG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-37_1696-35delGGG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-37_1034-35delGGG
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 4202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2643
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2029
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39863
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CGGG
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ

21-47957322-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957322
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957322
    reference: chr 21
allele count: 4386
allele frequency: 6.25802585395086e-2
allele num: 70086
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-37G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-37G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-37G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-37G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-37G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-37G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-37G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-37G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-37G>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 3.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 5183
  bin: 6.25e1
  variant carriers: 577
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 4.25e1
  variant carriers: 205
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 6.75e1
  variant carriers: 582
genotype depth: GenotypeDepth
  all individuals: 7673
  bin: 9.75e1
  variant carriers: 521
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 7.75e1
  variant carriers: 484
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 9.25e1
  variant carriers: 225
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 2.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 8.25e1
  variant carriers: 375
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 5.25e1
  variant carriers: 429
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4974
  bin: 5.75e1
  variant carriers: 524
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 7.25e1
  variant carriers: 520
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 4.75e1
  variant carriers: 305
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 8.75e1
  variant carriers: 299
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 9.25e1
  variant carriers: 143
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 8.75e1
  variant carriers: 121
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 7.5e0
  variant carriers: 214
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 7.25e1
  variant carriers: 144
genotype quality: GenotypeQuality
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 171
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 3.25e1
  variant carriers: 199
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

21-47957323-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957323
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957323
    reference: chr 21
allele count: 30
allele frequency: 2.500291700698415e-4
allele num: 119986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-36G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-36G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-36G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-36G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-36G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-36G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-36G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-36G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-36G>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5194
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4652
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum

21-47957324-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957324
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957324
    reference: chr 21
allele count: 1
allele frequency: 8.316284949187499e-6
allele num: 120246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-35G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-35G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-35G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-35G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-35G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-35G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-35G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-35G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-35G>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

21-47957325-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957325
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957325
    reference: chr 21
allele count: 13
allele frequency: 1.087847902127161e-4
allele num: 119502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-34C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-34C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-34C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-34C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-34C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-34C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-34C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-34C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-34C>G
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5188
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4013
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36974
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/21-47957325-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957325
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957325
    reference: chr 21
allele count: 52
allele frequency: 4.351391608508644e-4
allele num: 119502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-34C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-34C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-34C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-34C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-34C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-34C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-34C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-34C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-34C>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4013
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5188
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36974
  bin: 9.75e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 2457
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2048
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/21-47957328-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957328
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957328
    reference: chr 21
allele count: 210
allele frequency: 1.867862098409649e-3
allele num: 112428
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-31A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-31A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-31A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-31A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-31A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-31A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-31A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-31A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-31A>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 4.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 6.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 6.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 5.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 7.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2711
  bin: 2.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 3.75e1
  variant carriers: 8
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

21-47957330-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957330
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957330
    reference: chr 21
allele count: 7
allele frequency: 5.936530013399596e-5
allele num: 117914
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-29T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-29T>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5175
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2481
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: FS

21-47957332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957332
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957332
    reference: chr 21
allele count: 35728
allele frequency: 2.988640356013585e-1
allele num: 119546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-27G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-27G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-27G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-27G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-27G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-27G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-27G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-27G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-27G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 7.75e1
  variant carriers: 1827
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 1.75e1
  variant carriers: 685
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.25e1
  variant carriers: 282
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 6.25e1
  variant carriers: 2480
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 6.75e1
  variant carriers: 2331
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 2.25e1
  variant carriers: 861
genotype depth: GenotypeDepth
  all individuals: 5202
  bin: 4.75e1
  variant carriers: 1743
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 4.25e1
  variant carriers: 1111
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.25e1
  variant carriers: 1299
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 9.75e1
  variant carriers: 5520
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 5.75e1
  variant carriers: 2345
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 3.25e1
  variant carriers: 648
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 8.25e1
  variant carriers: 1669
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 5.25e1
  variant carriers: 2155
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 3.75e1
  variant carriers: 837
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 7.25e1
  variant carriers: 2104
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 2.75e1
  variant carriers: 794
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 8.75e1
  variant carriers: 1432
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 7.25e1
  variant carriers: 71
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 3.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 3.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 2.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 2.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.75e1
  variant carriers: 8
num of homozygotes: 5616
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

21-47957332-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957332
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957332
    reference: chr 21
allele count: 4
allele frequency: 3.345992337677547e-5
allele num: 119546
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-27G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-27G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-27G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-27G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-27G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-27G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-27G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-27G>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-27G>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD

21-47957336-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957336
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957336
    reference: chr 21
allele count: 5
allele frequency: 4.194701253376734e-5
allele num: 119198
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-23T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-23T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-23T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-23T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-23T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-23T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-23T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-23T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-23T>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6635
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5092
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2899
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2901
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32843
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ

21-47957337-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957337
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957337
    reference: chr 21
allele count: 4
allele frequency: 3.321707357581797e-5
allele num: 120420
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-22A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-22A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-22A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-22A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-22A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-22A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-22A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-22A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-22A>G
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3086
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2934
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

21-47957340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957340
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957340
    reference: chr 21
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-19C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-19C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-19C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-19C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-19C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-19C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-19C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-19C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-19C>T
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5411
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3643
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/21-47957341-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957341
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957341
    reference: chr 21
allele count: 1
allele frequency: 8.298066550493736e-6
allele num: 120510
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-18A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-18A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-18A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-18A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-18A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-18A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-18A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-18A>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-18A>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8735
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3674
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

21-47957341-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957341
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957341
    reference: chr 21
allele count: 1
allele frequency: 8.298066550493736e-6
allele num: 120510
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-18A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-18A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-18A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-18A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-18A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-18A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-18A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-18A>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-18A>G
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8735
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD

21-47957342-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957342
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957342
    reference: chr 21
allele count: 5
allele frequency: 4.149446463841723e-5
allele num: 120498
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-17T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-17T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-17T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-17T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-17T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-17T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-17T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-17T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-17T>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6843
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3095
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3682
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33318
  bin: 9.75e1
  variant carriers: 5
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

21-47957343-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957343
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957343
    reference: chr 21
allele count: 1
allele frequency: 8.298479718515568e-6
allele num: 120504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-16G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-16G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-16G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-16G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-16G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-16G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-16G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-16G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-16G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3679
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2936
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

21-47957344-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957344
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957344
    reference: chr 21
allele count: 1
allele frequency: 8.297928836962294e-6
allele num: 120512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-15T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-15T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-15T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-15T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-15T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-15T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-15T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-15T>C
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-15T>C
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4050
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3685
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

21-47957344-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957344
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957343
    reference: chr 21
allele count: 2
allele frequency: 1.659585767392459e-5
allele num: 120512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-14delG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-14delG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-14delG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-14delG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-14delG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-14delG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-14delG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-14delG
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-14delG
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4050
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2095
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2939
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2054
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: TG
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

21-47957352-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957352
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957352
    reference: chr 21
allele count: 1
allele frequency: 8.291598951941893e-6
allele num: 120604
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-7C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-7C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-7C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-7C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-7C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-7C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-7C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-7C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-7C>G
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3678
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9329
  bin: 6.25e1
  variant carriers: 0
hgvs: c.1708-7C>G
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS

http://identifiers.org/exac.variant/21-47957354-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957354
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957354
    reference: chr 21
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-5C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-5C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-5C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-5C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-5C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-5C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-5C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-5C>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-5C>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6830
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3092
  bin: 9.25e1
  variant carriers: 0
hgvs: c.1708-5C>A
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

21-47957354-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957354
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957354
    reference: chr 21
allele count: 83
allele frequency: 6.882141258022256e-4
allele num: 120602
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1034-5C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1579-5C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1711-5C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1708-5C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1696-5C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1708-5C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1101-5C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1516-5C>G
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1708-5C>G
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6830
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 7.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33338
  bin: 9.75e1
  variant carriers: 81
hgvs: c.1708-5C>G
num of homozygotes: 2
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

21-47957361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957361
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957361
    reference: chr 21
allele count: 4
allele frequency: 3.314221323699997e-5
allele num: 120692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1710C>T
  hgvsp: ENST00000435722.3:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1710C>T
  hgvsp: ENST00000457905.3:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1713C>T
  hgvsp: ENST00000318711.7:c.1713C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1581C>T
  hgvsp: ENST00000466639.1:c.1581C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1036C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1103C>T
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1698C>T
  hgvsp: ENST00000400274.1:c.1698C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1710C>T
  hgvsp: ENST00000417564.2:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1518C>T
  hgvsp: ENST00000427143.2:c.1518C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9733
  bin: 6.25e1
  variant carriers: 0
hgvs: c.1710C>T
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

21-47957362-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47957362
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 47957362
    reference: chr 21
allele count: 5
allele frequency: 4.141884391722858e-5
allele num: 120718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000415089
  ensembl transcript: ENST00000435722
  gene symbol: DIP2A
  hgvsc: ENST00000435722.3:c.1711G>A
  hgvsp: ENSP00000415089.3:p.Val571Ile
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000392066
  ensembl transcript: ENST00000417564
  gene symbol: DIP2A
  hgvsc: ENST00000417564.2:c.1711G>A
  hgvsp: ENSP00000392066.2:p.Val571Ile
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000393434
  ensembl transcript: ENST00000457905
  gene symbol: DIP2A
  hgvsc: ENST00000457905.3:c.1711G>A
  hgvsp: ENSP00000393434.3:p.Val571Ile
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000400528
  ensembl transcript: ENST00000427143
  gene symbol: DIP2A
  hgvsc: ENST00000427143.2:c.1519G>A
  hgvsp: ENSP00000400528.2:p.Val507Ile
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000430249
  ensembl transcript: ENST00000466639
  gene symbol: DIP2A
  hgvsc: ENST00000466639.1:c.1582G>A
  hgvsp: ENSP00000430249.1:p.Val528Ile
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000494435
  gene symbol: DIP2A
  hgvsc: ENST00000494435.1:n.1037G>A
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000323633
  ensembl transcript: ENST00000318711
  gene symbol: DIP2A
  hgvsc: ENST00000318711.7:c.1714G>A
  hgvsp: ENSP00000323633.7:p.Val572Ile
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160305
  ensembl protein: ENSP00000383133
  ensembl transcript: ENST00000400274
  gene symbol: DIP2A
  hgvsc: ENST00000400274.1:c.1699G>A
  hgvsp: ENSP00000383133.1:p.Val567Ile
  variant of: http://identifiers.org/hgnc/17217
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160305
  ensembl transcript: ENST00000473752
  gene symbol: DIP2A
  hgvsc: ENST00000473752.1:n.1104G>A
  variant of: http://identifiers.org/hgnc/17217
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Val571Ile
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3928
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3449
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46758
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9040
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.518055012384304e-5
allele num: 15342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10626
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62960
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 1.167e1

MQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

FS
type: SiteQuality
SIO_000300: 2.093e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.316267e6

GenotypeQuality
all individuals: 92
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51341
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 2.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16084
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530221882172915e-5
allele num: 65350
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.344e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

FS
type: SiteQuality
SIO_000300: 3.047e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

QD
type: SiteQuality
SIO_000300: 4.16e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

DP
type: SiteQuality
SIO_000300: 1.376764e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

GenotypeQuality
all individuals: 207
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51585
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3770
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 9.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527417137620284e-5
allele num: 65470
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11280
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16126
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.827e0

VQSLOD
type: SiteQuality
SIO_000300: -2.039e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.38081e6

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52188
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3868
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 309
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.035546246547066e-5
allele num: 65886
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: 6574
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.096e1

DP
type: SiteQuality
SIO_000300: 1.392703e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

VQSLOD
type: SiteQuality
SIO_000300: 8.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3861
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 975
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52060
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.762705923589205e-5
allele num: 11412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.657e1

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.168e0

FS
type: SiteQuality
SIO_000300: 6.581e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 1.394107e6

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3863
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 167
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 674
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52025
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517819197377208e-5
allele num: 65884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
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: 6580
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.226091221186856e-4
allele num: 16312
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.924e1

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.445e0

VQSLOD
type: SiteQuality
SIO_000300: 2.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 2.083e0

QD
type: SiteQuality
SIO_000300: 9.68e0

DP
type: SiteQuality
SIO_000300: 1.395427e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

GenotypeQuality
all individuals: 233
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 419
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51585
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.604794062176796e-5
allele num: 65748
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: 0
allele frequency: 0.0e0
allele num: 16286
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 1.393103e6

FS
type: SiteQuality
SIO_000300: 5.16e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

QD
type: SiteQuality
SIO_000300: 1.336e1

GenotypeQuality
all individuals: 90
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65084
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11238
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.208866261020738e-5
allele num: 16106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.064e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.16e-1

FS
type: SiteQuality
SIO_000300: 1.291e0

DP
type: SiteQuality
SIO_000300: 1.370519e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.46e0

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

MQ
type: SiteQuality
SIO_000300: 5.928e1

QD
type: SiteQuality
SIO_000300: 9.109999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.049e0

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

GenotypeQuality
all individuals: 90
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 415
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variant carriers: 1

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
all individuals: 8
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 269
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11238
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9354
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.208866261020738e-5
allele num: 16106
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65084
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.109999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -3.064e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.049e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.46e0

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

FS
type: SiteQuality
SIO_000300: 1.291e0

DP
type: SiteQuality
SIO_000300: 1.370519e6

MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.16e-1

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3535
bin: 6.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 82
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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
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 261
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variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 9.75e1
variant carriers: 67

GenotypeQuality
all individuals: 713
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.26017278076875e-5
allele num: 15974
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 8.348277781213283e-4
allele num: 64684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.702457956015524e-4
allele num: 9276
num of homozygotes: 0

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

Latino
type: Population
allele count: 4
allele frequency: 3.593890386343217e-4
allele num: 11130
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

QD
type: SiteQuality
SIO_000300: 1.295e1

DP
type: SiteQuality
SIO_000300: 1.360132e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

GenotypeQuality
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3515
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
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GenotypeQuality
all individuals: 99
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variant carriers: 0

GenotypeQuality
all individuals: 179
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variant carriers: 0

GenotypeQuality
all individuals: 465
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GenotypeQuality
all individuals: 3472
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variant carriers: 0

GenotypeQuality
all individuals: 406
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GenotypeQuality
all individuals: 572
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 543
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variant carriers: 0

GenotypeQuality
all individuals: 255
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GenotypeQuality
all individuals: 48634
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variant carriers: 0

GenotypeQuality
all individuals: 705
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variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 271
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.546742560168286e-5
allele num: 64652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15974
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9262
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 2.217e1

FS
type: SiteQuality
SIO_000300: 1.217e0

VQSLOD
type: SiteQuality
SIO_000300: -1.195e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.13e-1

DP
type: SiteQuality
SIO_000300: 1.359494e6

GenotypeQuality
all individuals: 272
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 590
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variant carriers: 0

GenotypeQuality
all individuals: 3497
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 254
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variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3838
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
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variant carriers: 0

GenotypeQuality
all individuals: 536
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variant carriers: 0

GenotypeQuality
all individuals: 565
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variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 9.75e1
variant carriers: 34

GenotypeQuality
all individuals: 48297
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 27
allele frequency: 3.220419847328244e-3
allele num: 8384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.302325581395349e-4
allele num: 6450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550339524355834e-5
allele num: 64502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15926
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

QD
type: SiteQuality
SIO_000300: 1.177e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.179e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.66e0

DP
type: SiteQuality
SIO_000300: 1.353373e6

GenotypeQuality
all individuals: 7910
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
all individuals: 1255
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GenotypeQuality
all individuals: 256
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variant carriers: 0

GenotypeQuality
all individuals: 594
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variant carriers: 0

GenotypeQuality
all individuals: 174
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GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 82
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GenotypeQuality
all individuals: 410
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variant carriers: 4

GenotypeQuality
all individuals: 524
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GenotypeQuality
all individuals: 42408
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GenotypeQuality
all individuals: 1088
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3163
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8886
num of homozygotes: 0

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

Latino
type: Population
allele count: 4
allele frequency: 3.820439350525311e-4
allele num: 10470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

FS
type: SiteQuality
SIO_000300: 1.729e0

DP
type: SiteQuality
SIO_000300: 1.284121e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.816e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.85e-1

GenotypeQuality
all individuals: 189
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 3104
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 290
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variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 5.25e1
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GenotypeQuality
all individuals: 611
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GenotypeQuality
all individuals: 515
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variant carriers: 0

GenotypeQuality
all individuals: 256
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GenotypeQuality
all individuals: 449
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GenotypeQuality
all individuals: 639
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variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41152
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8046
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15488
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: 0
allele frequency: 0.0e0
allele num: 8836
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.039102193067078e-5
allele num: 62196
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.2691e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.35e-1

DP
type: SiteQuality
SIO_000300: 1.27496e6

QD
type: SiteQuality
SIO_000300: 9.359999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.699e0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.75e1
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GenotypeQuality
all individuals: 516
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62164
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 9.05211431527221e-4
allele num: 15466
num of homozygotes: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.668e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.55e-1

QD
type: SiteQuality
SIO_000300: 1.031e1

VQSLOD
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SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 1.274203e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.616083260609587e-5
allele num: 61878
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: 1
allele frequency: 9.706853038245001e-5
allele num: 10302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6176
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.262498e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.54e-1

FS
type: SiteQuality
SIO_000300: 3.789e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.525e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.764e0

QD
type: SiteQuality
SIO_000300: 6.64e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 746
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7724
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5596
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.173158141717503e-4
allele num: 8524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54510
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

DP
type: SiteQuality
SIO_000300: 1.009854e6

MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 7.38e0

VQSLOD
type: SiteQuality
SIO_000300: -2.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.426e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 712
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.912411550965768e-5
allele num: 52290
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.095017022593624e-4
allele num: 6462
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.421262080727686e-4
allele num: 14072
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5400
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.513e0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.827e0

FS
type: SiteQuality
SIO_000300: 1.016e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

DP
type: SiteQuality
SIO_000300: 9.48465e5

QD
type: SiteQuality
SIO_000300: 3.039e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.991537939568116e-5
allele num: 50106
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

QD
type: SiteQuality
SIO_000300: 1.491e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.15e0

DP
type: SiteQuality
SIO_000300: 8.8421e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.32e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5872
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
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African
type: Population
allele count: 46
allele frequency: 6.733021077283372e-3
allele num: 6832
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.41282848262221e-4
allele num: 7078
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.068594596830913e-5
allele num: 48342
num of homozygotes: 0

South Asian
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allele count: 0
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.09e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 70

GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 1
allele frequency: 1.427755568246716e-4
allele num: 7004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 58
allele frequency: 1.141732283464567e-2
allele num: 5080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 1
allele frequency: 1.479289940828402e-3
allele num: 676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.91836904861169e-4
allele num: 47972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4820
num of homozygotes: 0

Other
type: Population
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.568381430363864e-4
allele num: 6376
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 45292
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MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
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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
all individuals: 161
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11598
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: 5290
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4040
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e0

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 1.32e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.25991e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.75e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 5.25e1
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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: 2.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.040399918384003e-4
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.389999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.163e0

DP
type: SiteQuality
SIO_000300: 8.133947e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.48e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.028100775193798e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 8.135109e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

FS
type: SiteQuality
SIO_000300: 6.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

QD
type: SiteQuality
SIO_000300: 1.358e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.35e0

GenotypeQuality
all individuals: 0
bin: 4.75e1
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
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.38e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

FS
type: SiteQuality
SIO_000300: 2.382e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.78e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

MQRankSum
type: SiteQuality
SIO_000300: -1.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 8.135372e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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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
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.852e0

QD
type: SiteQuality
SIO_000300: 1.221e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 1.835e0

MQRankSum
type: SiteQuality
SIO_000300: -1.962e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.139e0

VQSLOD
type: SiteQuality
SIO_000300: -7.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

DP
type: SiteQuality
SIO_000300: 8.135403e6

GenotypeQuality
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bin: 2.25e1
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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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1
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variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 3.059975520195838e-4
allele num: 9804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.08e-1

DP
type: SiteQuality
SIO_000300: 8.135799e6

VQSLOD
type: SiteQuality
SIO_000300: 2.82e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.976e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

QD
type: SiteQuality
SIO_000300: 1.48e1

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: 8626
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.4e-1

MQ
type: SiteQuality
SIO_000300: 5.995e1

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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 2.039983680130559e-4
allele num: 9804
num of homozygotes: 0

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

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

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

South Asian
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QD
type: SiteQuality
SIO_000300: 1.214e1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -7.66e-1

FS
type: SiteQuality
SIO_000300: 5.31e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.122e0

VQSLOD
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.993407252022775e-5
allele num: 66740
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 8.1364e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.95e0

MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

ReadPosRankSum
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QD
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele frequency: 7.491759065028469e-5
allele num: 66740
num of homozygotes: 0

East Asian
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allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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FS
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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SIO_000300: -3.66e-1

VQSLOD
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MQ
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GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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African
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South Asian
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East Asian
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MQRankSum
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.992e1

BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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FS
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

South Asian
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Other
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East Asian
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allele frequency: 1.159285879897983e-4
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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African
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FS
type: SiteQuality
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ClippingRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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ReadPosRankSum
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QD
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VQSLOD
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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Latino
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South Asian
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African
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European (Non-Finnish)
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QD
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MQ
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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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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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 15
allele frequency: 1.529363784665579e-3
allele num: 9808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.77e-1

InbreedingCoeff
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QD
type: SiteQuality
SIO_000300: 1.329e1

MQRankSum
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BaseQRankSum
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SIO_000300: -5.753e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.137312e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

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

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

MQRankSum
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SIO_000300: 1.9e0

MQ
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BaseQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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QD
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VQSLOD
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SIO_000300: -1.897e0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.988e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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QD
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SIO_000300: 1.619e1

VQSLOD
type: SiteQuality
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FS
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SIO_000300: 1.707e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
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SIO_000300: -7.31e-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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.048846269103986e-4
allele num: 66740
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.16e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.832e0

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 5.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.97e-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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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 56
allele frequency: 8.390770152831885e-4
allele num: 66740
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 103
allele frequency: 1.557302691260962e-2
allele num: 6614
num of homozygotes: 1

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

Other
type: Population
allele count: 3
allele frequency: 3.34075723830735e-3
allele num: 898
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.97e-2

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.32e-1

QD
type: SiteQuality
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DP
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VQSLOD
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BaseQRankSum
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SIO_000300: -6.832e0

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.16e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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African
type: Population
allele count: 3
allele frequency: 3.058103975535168e-4
allele num: 9810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

DP
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.505e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
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Latino
type: Population
allele count: 1
allele frequency: 8.922198429693076e-5
allele num: 11208
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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African
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allele count: 2
allele frequency: 2.076843198338525e-4
allele num: 9630
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South Asian
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

VQSLOD
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QD
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.217e0

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

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

South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 0
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African
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allele count: 0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.526904049349539e-5
allele num: 65492
num of homozygotes: 0

MQRankSum
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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SIO_000300: 4.527395e6

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.5956e1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.765e1

GenotypeQuality
all individuals: 1124
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variant carriers: 184

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1013
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GenotypeQuality
all individuals: 1047
bin: 4.75e1
variant carriers: 184

Latino
type: Population
allele count: 596
allele frequency: 1.406987724268177e-1
allele num: 4236
num of homozygotes: 0

Other
type: Population
allele count: 18
allele frequency: 3.703703703703703e-2
allele num: 486
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East Asian
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allele count: 599
allele frequency: 1.361982719417917e-1
allele num: 4398
num of homozygotes: 0

South Asian
type: Population
allele count: 329
allele frequency: 3.293293293293293e-2
allele num: 9990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2139
allele frequency: 4.863795534130701e-2
allele num: 43978
num of homozygotes: 0

African
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allele count: 396
allele frequency: 8.753315649867374e-2
allele num: 4524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 309
allele frequency: 1.248989490703314e-1
allele num: 2474
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

FS
type: SiteQuality
SIO_000300: 1.27307e2

VQSLOD
type: SiteQuality
SIO_000300: -7.644e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.59e-1

QD
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 5.88e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.952e0

DP
type: SiteQuality
SIO_000300: 3.925368e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.057e0

GenotypeQuality
all individuals: 611
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 36854
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 126
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 247
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1934
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2474
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2100
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2665
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2576
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.321262766945218e-4
allele num: 8616
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.835625979453248e-4
allele num: 11486
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.025430680885972e-4
allele num: 9752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.260397830018083e-4
allele num: 66360
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.225640397107489e-4
allele num: 16318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.522533495736906e-4
allele num: 6568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.198e0

QD
type: SiteQuality
SIO_000300: 2.15e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

VQSLOD
type: SiteQuality
SIO_000300: -2.096e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.556e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

DP
type: SiteQuality
SIO_000300: 3.543217e6

FS
type: SiteQuality
SIO_000300: 6.3496e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

GenotypeQuality
all individuals: 625
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37081
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4295
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2515
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2699
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 388
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1958
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66450
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.133464180569185e-5
allele num: 16304
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.893000000000001e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

DP
type: SiteQuality
SIO_000300: 3.538759e6

MQRankSum
type: SiteQuality
SIO_000300: -6.03e-1

QD
type: SiteQuality
SIO_000300: 3.57e0

FS
type: SiteQuality
SIO_000300: 1.44941e2

MQ
type: SiteQuality
SIO_000300: 5.833e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.206e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.372e0

GenotypeQuality
all individuals: 2048
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2777
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4128
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 214
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2522
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 452
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 623
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2660
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 689
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2457
bin: 8.25e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 1.021867974657674e-4
allele num: 9786
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.051685122046888e-5
allele num: 66286
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.267909217700013e-4
allele num: 15774
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.597402597402597e-4
allele num: 11550
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.082e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

QD
type: SiteQuality
SIO_000300: 1.171e1

DP
type: SiteQuality
SIO_000300: 3.533445e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.352e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

GenotypeQuality
all individuals: 131
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4128
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2660
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 49
allele frequency: 5.007153075822604e-3
allele num: 9786
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.017228374015629e-5
allele num: 66286
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

DP
type: SiteQuality
SIO_000300: 3.533445e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.352e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 7.082e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

QD
type: SiteQuality
SIO_000300: 1.171e1

GenotypeQuality
all individuals: 840
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 512
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2210
bin: 7.75e1
variant carriers: 9

GenotypeQuality
all individuals: 895
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 863
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 32216
bin: 9.75e1
variant carriers: 128

GenotypeQuality
all individuals: 875
bin: 5.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2246
bin: 9.25e1
variant carriers: 6

GenotypeQuality
all individuals: 2111
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1044
bin: 2.25e1
variant carriers: 6

GenotypeQuality
all individuals: 913
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1858
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1692
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4051
bin: 6.25e1
variant carriers: 4

European (Finnish)
type: Population
allele count: 14
allele frequency: 2.452697967764541e-3
allele num: 5708
num of homozygotes: 0

South Asian
type: Population
allele count: 21
allele frequency: 1.411480037639468e-3
allele num: 14878
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 1.85293543982836e-3
allele num: 10254
num of homozygotes: 0

African
type: Population
allele count: 18
allele frequency: 1.944684528954192e-3
allele num: 9256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 106
allele frequency: 1.670501465628644e-3
allele num: 63454
num of homozygotes: 0

East Asian
type: Population
allele count: 32
allele frequency: 3.974167908594138e-3
allele num: 8052
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.101e0

FS
type: SiteQuality
SIO_000300: 5.7763e1

DP
type: SiteQuality
SIO_000300: 3.565089e6

QD
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.31e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.99e-1

MQ
type: SiteQuality
SIO_000300: 5.871e1

VQSLOD
type: SiteQuality
SIO_000300: -1.69e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.598e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-1

GenotypeQuality
all individuals: 2604
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2565
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3012
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 829
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 509
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34751
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 692
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1939
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 177
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4807
bin: 6.25e1
variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 1.0315659170621e-4
allele num: 9694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.047015448368323e-5
allele num: 65638
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.34796900680911e-4
allele num: 8518
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.252975817566721e-4
allele num: 15962
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.571e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.732e0

VQSLOD
type: SiteQuality
SIO_000300: -1.377e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

QD
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 5.861e1

DP
type: SiteQuality
SIO_000300: 3.513975e6

FS
type: SiteQuality
SIO_000300: 4.9772e1

GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 43203
bin: 9.75e1
variant carriers: 29415

GenotypeQuality
all individuals: 1292
bin: 8.75e1
variant carriers: 66

GenotypeQuality
all individuals: 170
bin: 7.5e0
variant carriers: 8

GenotypeQuality
all individuals: 2146
bin: 6.75e1
variant carriers: 76

GenotypeQuality
all individuals: 1689
bin: 8.25e1
variant carriers: 95

GenotypeQuality
all individuals: 311
bin: 5.75e1
variant carriers: 57

GenotypeQuality
all individuals: 3838
bin: 6.25e1
variant carriers: 59

GenotypeQuality
all individuals: 321
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 1800
bin: 7.75e1
variant carriers: 68

GenotypeQuality
all individuals: 306
bin: 4.75e1
variant carriers: 37

GenotypeQuality
all individuals: 287
bin: 4.25e1
variant carriers: 28

GenotypeQuality
all individuals: 286
bin: 5.25e1
variant carriers: 53

GenotypeQuality
all individuals: 1690
bin: 9.25e1
variant carriers: 71

European (Non-Finnish)
type: Population
allele count: 21655
allele frequency: 3.26611565261983e-1
allele num: 66302
num of homozygotes: 3523

South Asian
type: Population
allele count: 4316
allele frequency: 2.674433015243525e-1
allele num: 16138
num of homozygotes: 590

Latino
type: Population
allele count: 2419
allele frequency: 2.112294795668879e-1
allele num: 11452
num of homozygotes: 281

African
type: Population
allele count: 1450
allele frequency: 1.483224222585925e-1
allele num: 9776
num of homozygotes: 80

Other
type: Population
allele count: 273
allele frequency: 3.088235294117647e-1
allele num: 884
num of homozygotes: 47

East Asian
type: Population
allele count: 3791
allele frequency: 4.426669780476413e-1
allele num: 8564
num of homozygotes: 854

European (Finnish)
type: Population
allele count: 1824
allele frequency: 2.836702954898911e-1
allele num: 6430
num of homozygotes: 241

DP
type: SiteQuality
SIO_000300: 3.550373e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e0

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

FS
type: SiteQuality
SIO_000300: 3.202e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.757e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.76e-2

GenotypeQuality
all individuals: 370
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43203
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 170
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1690
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3838
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2146
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.196554715578138e-5
allele num: 16138
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.555209953343701e-4
allele num: 6430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.335357309668379e-4
allele num: 8564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66302
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

DP
type: SiteQuality
SIO_000300: 3.550373e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.76e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 3.202e0

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.757e1

GenotypeQuality
all individuals: 7857
bin: 6.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 581
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2022
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2059
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.018122581958868e-4
allele num: 9822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.027727546714889e-5
allele num: 66360
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.361e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.212e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.935e0

VQSLOD
type: SiteQuality
SIO_000300: -1.722e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.011e0

DP
type: SiteQuality
SIO_000300: 2.948506e6

FS
type: SiteQuality
SIO_000300: 1.565e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.008893161879582e-5
allele num: 66568
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.023e1

FS
type: SiteQuality
SIO_000300: 8.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.575e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.611e0

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.295e0

MQ
type: SiteQuality
SIO_000300: 5.937e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 2.937661e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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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bin: 9.75e1
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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9824
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: 1
allele frequency: 1.502268425322237e-5
allele num: 66566
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16336
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 6.052e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.195e0

DP
type: SiteQuality
SIO_000300: 2.939078e6

VQSLOD
type: SiteQuality
SIO_000300: 8.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 460
bin: 2.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.612e0

QD
type: SiteQuality
SIO_000300: 1.388e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.73e-1

DP
type: SiteQuality
SIO_000300: 2.939889e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-1

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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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
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 33324
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501726986033939e-5
allele num: 66590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

DP
type: SiteQuality
SIO_000300: 2.939889e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 8.612e0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

MQRankSum
type: SiteQuality
SIO_000300: -2.16e-1

QD
type: SiteQuality
SIO_000300: 1.388e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

East Asian
type: Population
allele count: 5
allele frequency: 5.796429399489915e-4
allele num: 8626
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.548e0

DP
type: SiteQuality
SIO_000300: 2.94043e6

QD
type: SiteQuality
SIO_000300: 1.424e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502042778178322e-5
allele num: 66576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.940813e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: -3.426e-1

QD
type: SiteQuality
SIO_000300: 1.524e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.503e0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 5.033e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9832
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16394
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.083e1

FS
type: SiteQuality
SIO_000300: 1.536e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.23e0

DP
type: SiteQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 8985
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9832
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.219958521410272e-4
allele num: 16394
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

MQ
type: SiteQuality
SIO_000300: 6.083e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.23e0

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

FS
type: SiteQuality
SIO_000300: 1.536e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.941101e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

GenotypeQuality
all individuals: 351
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2932
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2938
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33328
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3095
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2056
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9838
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

DP
type: SiteQuality
SIO_000300: 2.946125e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.484e0

VQSLOD
type: SiteQuality
SIO_000300: 5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 2.856e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2054
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9404
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2934
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3695
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2936
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9840
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.942e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.371e0

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

DP
type: SiteQuality
SIO_000300: 2.948966e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.37e0

QD
type: SiteQuality
SIO_000300: 1.308e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2934
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2936
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2054
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3695
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9404
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3092
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002011347602894e-5
allele num: 66622
num of homozygotes: 0

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

East Asian
type: Population
allele count: 68
allele frequency: 7.881316643486324e-3
allele num: 8628
num of homozygotes: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9840
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.087909411907951e-4
allele num: 16426
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.371e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

DP
type: SiteQuality
SIO_000300: 2.948966e6

QD
type: SiteQuality
SIO_000300: 1.308e1

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33369
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2085
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3690
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2927
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2929
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3083
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.026753141467369e-4
allele num: 9868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000660145231951e-5
allele num: 66652
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.876e1

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.924e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.72e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

FS
type: SiteQuality
SIO_000300: 1.133e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.17e-1

DP
type: SiteQuality
SIO_000300: 2.931816e6