19-10928211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10928211
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10928211
    reference: chr 19
allele count: 1
allele frequency: 5.409499080385156e-5
allele num: 18486
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1660-2445C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1660-2445C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1672-2445C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1672-2445C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3860-2445C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3171-2445C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1672-2445C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1672-2445C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33429
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29668
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3027
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-10928219-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10928219
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10928219
    reference: chr 19
allele count: 1
allele frequency: 5.533421868083223e-5
allele num: 18072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3860-2437C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1672-2437C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1672-2437C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1660-2437C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1672-2437C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1660-2437C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1672-2437C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3171-2437C>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26880
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1841
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3366
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-10930607-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930607
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930607
    reference: chr 19
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1660-49G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3171-49G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1660-49G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1672-49G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1672-49G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1672-49G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3860-49G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1672-49G>C
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19767
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3183
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

19-10930616-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930616
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930616
    reference: chr 19
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1660-40C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1660-40C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1672-40C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3171-40C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1672-40C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1672-40C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3860-40C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1672-40C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

19-10930617-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930617
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930617
    reference: chr 19
allele count: 44
allele frequency: 3.625337815569178e-4
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1660-39G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3171-39G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1672-39G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3860-39G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1672-39G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1660-39G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1672-39G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1672-39G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16132
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5835
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8886
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

19-10930623-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930623
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930623
    reference: chr 19
allele count: 50
allele frequency: 4.119769952045878e-4
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1672-33C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1672-33C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1672-33C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1660-33C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3860-33C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1660-33C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1672-33C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3171-33C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16467
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8900
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4091
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-10930629-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930629
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930629
    reference: chr 19
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1660-27G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1672-27G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3860-27G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1660-27G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1672-27G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1672-27G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1672-27G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3171-27G>C
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3185
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

19-10930635-CTCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930635
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930631
    reference: chr 19
allele count: 6
allele frequency: 4.943398091848337e-5
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1660-19_1660-16delCTTT
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1672-19_1672-16delCTTT
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1660-19_1660-16delCTTT
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1672-19_1672-16delCTTT
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3860-19_3860-16delCTTT
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3171-19_3171-16delCTTT
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1672-19_1672-16delCTTT
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1672-19_1672-16delCTTT
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9094
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16162
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13204
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20149
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4091
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: CTCTT
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

19-10930640-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930640
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930640
    reference: chr 19
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1672-16T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3171-16T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1672-16T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1660-16T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1660-16T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1672-16T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1672-16T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3860-16T>C
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16167
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8926
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3182
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5222
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

19-10930641-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930641
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930642
    reference: chr 19
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3171-12dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3860-12dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1672-12dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1672-12dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1672-12dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1672-12dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1660-12dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1660-12dupC
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3702
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3183
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-10930696-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930696
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930696
    reference: chr 19
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3900A>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3211A>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1700A>G
  hgvsp: ENSP00000352721.6:p.Lys567Arg
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1700A>G
  hgvsp: ENSP00000386192.3:p.Lys567Arg
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1712A>G
  hgvsp: ENSP00000468734.1:p.Lys571Arg
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1712A>G
  hgvsp: ENSP00000373905.3:p.Lys571Arg
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1712A>G
  hgvsp: ENSP00000347890.6:p.Lys571Arg
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1712A>G
  hgvsp: ENSP00000313164.5:p.Lys571Arg
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3182
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys571Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

19-10930698-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930698
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930698
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1702A>G
  hgvsp: ENSP00000386192.3:p.Ile568Val
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1714A>G
  hgvsp: ENSP00000313164.5:p.Ile572Val
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1714A>G
  hgvsp: ENSP00000347890.6:p.Ile572Val
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3902A>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1714A>G
  hgvsp: ENSP00000373905.3:p.Ile572Val
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1702A>G
  hgvsp: ENSP00000352721.6:p.Ile568Val
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1714A>G
  hgvsp: ENSP00000468734.1:p.Ile572Val
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3213A>G
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20298
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile572Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/19-10930700-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930700
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930700
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1704C>A
  hgvsp: ENST00000359692.6:c.1704C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1716C>A
  hgvsp: ENST00000355667.6:c.1716C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1716C>A
  hgvsp: ENST00000585892.1:c.1716C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3215C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1704C>A
  hgvsp: ENST00000408974.4:c.1704C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3904C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1716C>A
  hgvsp: ENST00000389253.4:c.1716C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1716C>A
  hgvsp: ENST00000314646.5:c.1716C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5214
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8939
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile572Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP

19-10930715-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930715
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930715
    reference: chr 19
allele count: 2
allele frequency: 1.647880825258717e-5
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3230G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1731G>A
  hgvsp: ENST00000389253.4:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1731G>A
  hgvsp: ENST00000585892.1:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1731G>A
  hgvsp: ENST00000314646.5:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1719G>A
  hgvsp: ENST00000408974.4:c.1719G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1731G>A
  hgvsp: ENST00000355667.6:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1719G>A
  hgvsp: ENST00000359692.6:c.1719G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3919G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16564
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3699
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys577Lys
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-10930718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930718
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930718
    reference: chr 19
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1734C>T
  hgvsp: ENST00000389253.4:c.1734C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1734C>T
  hgvsp: ENST00000585892.1:c.1734C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1722C>T
  hgvsp: ENST00000359692.6:c.1722C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1734C>T
  hgvsp: ENST00000314646.5:c.1734C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1722C>T
  hgvsp: ENST00000408974.4:c.1722C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3922C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3233C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1734C>T
  hgvsp: ENST00000355667.6:c.1734C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5210
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13198
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3699
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly578Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-10930736-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930736
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930736
    reference: chr 19
allele count: 9
allele frequency: 7.418275333410263e-5
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1752C>T
  hgvsp: ENST00000314646.5:c.1752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1752C>T
  hgvsp: ENST00000389253.4:c.1752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1752C>T
  hgvsp: ENST00000355667.6:c.1752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1740C>T
  hgvsp: ENST00000408974.4:c.1740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3940C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3251C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1752C>T
  hgvsp: ENST00000585892.1:c.1752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1740C>T
  hgvsp: ENST00000359692.6:c.1740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16549
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4084
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3687
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13198
  bin: 9.75e1
  variant carriers: 9
hgvs: p.His584His
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

19-10930737-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930737
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930737
    reference: chr 19
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1753G>A
  hgvsp: ENSP00000347890.6:p.Val585Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1753G>A
  hgvsp: ENSP00000468734.1:p.Val585Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3252G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3941G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1741G>A
  hgvsp: ENSP00000352721.6:p.Val581Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1741G>A
  hgvsp: ENSP00000386192.3:p.Val581Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1753G>A
  hgvsp: ENSP00000373905.3:p.Val585Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1753G>A
  hgvsp: ENSP00000313164.5:p.Val585Ile
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5208
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20251
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val585Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

19-10930742-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930742
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930742
    reference: chr 19
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3946C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3257C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1746C>T
  hgvsp: ENST00000408974.4:c.1746C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1758C>T
  hgvsp: ENST00000355667.6:c.1758C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1758C>T
  hgvsp: ENST00000314646.5:c.1758C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1746C>T
  hgvsp: ENST00000359692.6:c.1746C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1758C>T
  hgvsp: ENST00000585892.1:c.1758C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1758C>T
  hgvsp: ENST00000389253.4:c.1758C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8911
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe586Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ

19-10930757-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930757
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930757
    reference: chr 19
allele count: 2
allele frequency: 1.649756660892518e-5
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3961G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1773G>A
  hgvsp: ENST00000314646.5:c.1773G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1761G>A
  hgvsp: ENST00000359692.6:c.1761G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1773G>A
  hgvsp: ENST00000355667.6:c.1773G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3272G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1773G>A
  hgvsp: ENST00000585892.1:c.1773G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1773G>A
  hgvsp: ENST00000389253.4:c.1773G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1761G>A
  hgvsp: ENST00000408974.4:c.1761G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3679
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3182
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr591Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

19-10930758-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930758
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930758
    reference: chr 19
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1774G>A
  hgvsp: ENSP00000313164.5:p.Glu592Lys
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1774G>A
  hgvsp: ENSP00000373905.3:p.Glu592Lys
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1774G>A
  hgvsp: ENSP00000468734.1:p.Glu592Lys
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1762G>A
  hgvsp: ENSP00000386192.3:p.Glu588Lys
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1762G>A
  hgvsp: ENSP00000352721.6:p.Glu588Lys
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1774G>A
  hgvsp: ENSP00000347890.6:p.Glu592Lys
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3962G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3273G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5201
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu592Lys
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: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ

19-10930772-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930772
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930772
    reference: chr 19
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1769+7G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1781+7G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1781+7G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1781+7G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1781+7G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3969+7G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1769+7G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3280+7G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13186
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3656
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1781+7G>A
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

19-10930781-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930781
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930781
    reference: chr 19
allele count: 1
allele frequency: 8.275131574592036e-6
allele num: 120844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1769+16G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1781+16G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1781+16G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3969+16G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1769+16G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3280+16G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1781+16G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1781+16G>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5161
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3621
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/19-10930782-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930782
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930782
    reference: chr 19
allele count: 76
allele frequency: 6.288995912152657e-4
allele num: 120846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1781+17C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1781+17C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1769+17C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3969+17C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1769+17C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3280+17C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1781+17C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1781+17C>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 16227
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15934
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9011
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 5.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 5157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4053
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-10930783-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930783
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930783
    reference: chr 19
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1781+18C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1769+18C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3280+18C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1769+18C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3969+18C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1781+18C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1781+18C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1781+18C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15853
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8617
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4054
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

19-10930791-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930791
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930791
    reference: chr 19
allele count: 1
allele frequency: 8.296276631047985e-6
allele num: 120536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1781+26G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1769+26G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1781+26G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1769+26G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1781+26G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3280+26G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3969+26G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1781+26G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3379
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1259
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

19-10930793-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930793
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930793
    reference: chr 19
allele count: 1
allele frequency: 8.300959590928711e-6
allele num: 120468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1781+28C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3969+28C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1781+28C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3280+28C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1781+28C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1769+28C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1769+28C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1781+28C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14757
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-10930795-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930795
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930795
    reference: chr 19
allele count: 2
allele frequency: 1.661212352775055e-5
allele num: 120394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1781+30C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1781+30C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3969+30C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1769+30C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1781+30C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1769+30C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1781+30C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3280+30C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3139
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

19-10930796-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930796
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930796
    reference: chr 19
allele count: 2
allele frequency: 1.662178783950002e-5
allele num: 120324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1781+31G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1781+31G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1769+31G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3280+31G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3969+31G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1781+31G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1769+31G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1781+31G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14234
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17299
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4895
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3334
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

19-10930801-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930801
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930801
    reference: chr 19
allele count: 5
allele frequency: 4.161464835622139e-5
allele num: 120150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1781+36G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1769+36G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3969+36G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3280+36G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1769+36G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1781+36G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1781+36G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1781+36G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14345
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5555
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4782
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6919
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1993
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

19-10930809-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10930809
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10930809
    reference: chr 19
allele count: 38
allele frequency: 3.171476739721911e-4
allele num: 119818
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3280+44A>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1781+44A>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1769+44A>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1781+44A>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3969+44A>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1769+44A>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1781+44A>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1781+44A>G
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11584
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12098
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5890
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3872
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1398
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4698
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

19-10934418-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934418
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934418
    reference: chr 19
allele count: 2
allele frequency: 1.67740203972088e-5
allele num: 119232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.519C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1782-46C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1770-46C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1770-46C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1782-46C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3281-46C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1782-46C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3970-46C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1782-46C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9050
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2724
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-10934452-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934452
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934453
    reference: chr 19
allele count: 78
allele frequency: 6.586725215335247e-4
allele num: 118420
alternate allele: AC
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3281-5dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1782-5dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.560dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1782-5dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1770-5dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1770-5dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1782-5dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1782-5dupC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3970-5dupC
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12122
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 22786
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9958
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 4.75e1
  variant carriers: 8
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-10934452-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934452
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934451
    reference: chr 19
allele count: 4
allele frequency: 3.377807802736024e-5
allele num: 118420
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3970-5delC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1782-5delC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1770-5delC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1782-5delC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1782-5delC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.560delC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1782-5delC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3281-5delC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1770-5delC
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22786
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: AC
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/19-10934453-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934453
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934453
    reference: chr 19
allele count: 1
allele frequency: 8.439245868989148e-6
allele num: 118494
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1782-11C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.554C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1770-11C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3970-11C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1782-11C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1782-11C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3281-11C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1770-11C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1782-11C>A
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1555
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33640
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

19-10934453-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934453
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934453
    reference: chr 19
allele count: 336
allele frequency: 2.835586611980353e-3
allele num: 118494
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1782-11C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1770-11C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1782-11C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1770-11C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.554C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1782-11C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3281-11C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3970-11C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1782-11C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22931
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 5.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 4.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12078
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 9991
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1555
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2503
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 2.25e1
  variant carriers: 1
num of homozygotes: 4
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

19-10934456-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934456
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934456
    reference: chr 19
allele count: 1
allele frequency: 8.374507997655138e-6
allele num: 119410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3970-8C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1782-8C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1770-8C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1770-8C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.557C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1782-8C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3281-8C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1782-8C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1782-8C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1782-8C>T
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-10934457-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934457
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934457
    reference: chr 19
allele count: 5
allele frequency: 4.187885285446261e-5
allele num: 119392
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1782-7C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3281-7C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1782-7C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3970-7C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1770-7C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1770-7C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1782-7C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1782-7C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.558C>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5966
  bin: 9.75e1
  variant carriers: 5
hgvs: c.1782-7C>A
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

19-10934457-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934457
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934457
    reference: chr 19
allele count: 2
allele frequency: 1.675154114178504e-5
allele num: 119392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1782-7C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1782-7C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1782-7C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3970-7C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.558C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1770-7C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3281-7C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1782-7C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1770-7C>G
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34577
  bin: 6.25e1
  variant carriers: 0
hgvs: c.1782-7C>G
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

19-10934459-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934459
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934459
    reference: chr 19
allele count: 28
allele frequency: 2.345137190525646e-4
allele num: 119396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1770-5C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1782-5C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1782-5C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3281-5C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1782-5C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1782-5C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.560C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1770-5C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3970-5C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10186
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2843
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1782-5C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

19-10934460-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934460
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934460
    reference: chr 19
allele count: 4
allele frequency: 3.352610845696086e-5
allele num: 119310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.561G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1782-4G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1770-4G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3281-4G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3970-4G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1770-4G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1782-4G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1782-4G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1782-4G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5942
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9124
  bin: 6.75e1
  variant carriers: 0
hgvs: c.1782-4G>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

19-10934460-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934460
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934460
    reference: chr 19
allele count: 4
allele frequency: 3.352610845696086e-5
allele num: 119310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3281-4G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3970-4G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1782-4G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1770-4G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1782-4G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1782-4G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1770-4G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1782-4G>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.561G>C
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2545
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1782-4G>C
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

19-10934467-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934467
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934467
    reference: chr 19
allele count: 2
allele frequency: 1.673220112105748e-5
allele num: 119530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.568C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1785C>T
  hgvsp: ENST00000355667.6:c.1785C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1785C>T
  hgvsp: ENST00000389253.4:c.1785C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1785C>T
  hgvsp: ENST00000314646.5:c.1785C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1773C>T
  hgvsp: ENST00000359692.6:c.1773C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1785C>T
  hgvsp: ENST00000585892.1:c.1785C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3284C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3973C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1773C>T
  hgvsp: ENST00000408974.4:c.1773C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9157
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn595Asn
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

19-10934468-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934468
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934468
    reference: chr 19
allele count: 3
allele frequency: 2.508822693137534e-5
allele num: 119578
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1786G>A
  hgvsp: ENSP00000373905.3:p.Val596Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3285G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1786G>A
  hgvsp: ENSP00000468734.1:p.Val596Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3974G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.569G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1774G>A
  hgvsp: ENSP00000386192.3:p.Val592Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1786G>A
  hgvsp: ENSP00000347890.6:p.Val596Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1774G>A
  hgvsp: ENSP00000352721.6:p.Val592Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1786G>A
  hgvsp: ENSP00000313164.5:p.Val596Ile
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5938
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val596Ile
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

19-10934480-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934480
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934480
    reference: chr 19
allele count: 1
allele frequency: 8.356452852893003e-6
allele num: 119668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1798C>T
  hgvsp: ENST00000585892.1:c.1798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.581C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1798C>T
  hgvsp: ENST00000314646.5:c.1798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3986C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1786C>T
  hgvsp: ENST00000408974.4:c.1786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1798C>T
  hgvsp: ENST00000389253.4:c.1798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3297C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1786C>T
  hgvsp: ENST00000359692.6:c.1786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1798C>T
  hgvsp: ENST00000355667.6:c.1798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9180
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu600Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-10934484-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934484
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934484
    reference: chr 19
allele count: 1
allele frequency: 8.354498061756449e-6
allele num: 119696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1802G>A
  hgvsp: ENSP00000347890.6:p.Arg601Gln
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1802G>A
  hgvsp: ENSP00000373905.3:p.Arg601Gln
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1802G>A
  hgvsp: ENSP00000313164.5:p.Arg601Gln
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1790G>A
  hgvsp: ENSP00000352721.6:p.Arg597Gln
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1802G>A
  hgvsp: ENSP00000468734.1:p.Arg601Gln
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3301G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.585G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1790G>A
  hgvsp: ENSP00000386192.3:p.Arg597Gln
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3990G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2566
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35251
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg601Gln
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

19-10934491-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934491
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934491
    reference: chr 19
allele count: 1
allele frequency: 8.345294922722569e-6
allele num: 119828
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1809C>G
  hgvsp: ENSP00000313164.5:p.Ile603Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.592C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1797C>G
  hgvsp: ENSP00000386192.3:p.Ile599Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1809C>G
  hgvsp: ENSP00000373905.3:p.Ile603Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3308C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1809C>G
  hgvsp: ENSP00000468734.1:p.Ile603Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1809C>G
  hgvsp: ENSP00000347890.6:p.Ile603Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1797C>G
  hgvsp: ENSP00000352721.6:p.Ile599Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.3997C>G
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5935
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 925
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile603Met
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

19-10934500-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934500
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934500
    reference: chr 19
allele count: 1
allele frequency: 8.334305668994715e-6
allele num: 119986
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1806C>G
  hgvsp: ENST00000359692.6:c.1806C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.601C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1818C>G
  hgvsp: ENST00000314646.5:c.1818C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3317C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4006C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1818C>G
  hgvsp: ENST00000355667.6:c.1818C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1806C>G
  hgvsp: ENST00000408974.4:c.1806C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1818C>G
  hgvsp: ENST00000585892.1:c.1818C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1818C>G
  hgvsp: ENST00000389253.4:c.1818C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35664
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2566
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala606Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum

19-10934509-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934509
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934509
    reference: chr 19
allele count: 8
allele frequency: 6.666666666666667e-5
allele num: 120000
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1815C>T
  hgvsp: ENST00000359692.6:c.1815C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4015C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3326C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1815C>T
  hgvsp: ENST00000408974.4:c.1815C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.610C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1827C>T
  hgvsp: ENST00000585892.1:c.1827C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1827C>T
  hgvsp: ENST00000355667.6:c.1827C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  clinical significance: uncertain_significance
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1827C>T
  hgvsp: ENST00000389253.4:c.1827C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1827C>T
  hgvsp: ENST00000314646.5:c.1827C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1577
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser609Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

19-10934518-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934518
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934518
    reference: chr 19
allele count: 3
allele frequency: 2.499375156210947e-5
allele num: 120030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1836C>T
  hgvsp: ENST00000355667.6:c.1836C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1836C>T
  hgvsp: ENST00000389253.4:c.1836C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1836C>T
  hgvsp: ENST00000585892.1:c.1836C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3335C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1824C>T
  hgvsp: ENST00000359692.6:c.1824C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1824C>T
  hgvsp: ENST00000408974.4:c.1824C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1836C>T
  hgvsp: ENST00000314646.5:c.1836C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.619C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4024C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23841
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9200
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp612Asp
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

19-10934519-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934519
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934519
    reference: chr 19
allele count: 29
allele frequency: 2.416263956007332e-4
allele num: 120020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1825G>A
  hgvsp: ENSP00000352721.6:p.Val609Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1837G>A
  hgvsp: ENSP00000313164.5:p.Val613Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1837G>A
  hgvsp: ENSP00000347890.6:p.Val613Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3336G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1837G>A
  hgvsp: ENSP00000373905.3:p.Val613Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1837G>A
  hgvsp: ENSP00000468734.1:p.Val613Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1825G>A
  hgvsp: ENSP00000386192.3:p.Val609Met
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.620G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4025G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 12154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10811
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35768
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val613Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

19-10934521-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934521
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934521
    reference: chr 19
allele count: 2
allele frequency: 1.666222340709144e-5
allele num: 120032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3338G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1839G>T
  hgvsp: ENST00000355667.6:c.1839G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1839G>T
  hgvsp: ENST00000314646.5:c.1839G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1839G>T
  hgvsp: ENST00000389253.4:c.1839G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1827G>T
  hgvsp: ENST00000359692.6:c.1827G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1839G>T
  hgvsp: ENST00000585892.1:c.1839G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4027G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1827G>T
  hgvsp: ENST00000408974.4:c.1827G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.622G>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2559
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val613Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

19-10934534-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934534
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934534
    reference: chr 19
allele count: 1
allele frequency: 8.3380582329987e-6
allele num: 119932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1840G>T
  hgvsp: ENSP00000352721.6:p.Ala614Ser
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1852G>T
  hgvsp: ENSP00000373905.3:p.Ala618Ser
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1852G>T
  hgvsp: ENSP00000313164.5:p.Ala618Ser
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1852G>T
  hgvsp: ENSP00000468734.1:p.Ala618Ser
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1840G>T
  hgvsp: ENSP00000386192.3:p.Ala614Ser
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3351G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1852G>T
  hgvsp: ENSP00000347890.6:p.Ala618Ser
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.635G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4040G>T
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala618Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-10934539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934539
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934539
    reference: chr 19
allele count: 4
allele frequency: 3.337449521075993e-5
allele num: 119852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1845G>A
  hgvsp: ENST00000359692.6:c.1845G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1857G>A
  hgvsp: ENST00000355667.6:c.1857G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3356G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1857G>A
  hgvsp: ENST00000585892.1:c.1857G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1845G>A
  hgvsp: ENST00000408974.4:c.1845G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.640G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4045G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1857G>A
  hgvsp: ENST00000389253.4:c.1857G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1857G>A
  hgvsp: ENST00000314646.5:c.1857G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser619Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

19-10934539-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934539
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934539
    reference: chr 19
allele count: 2
allele frequency: 1.668724760537997e-5
allele num: 119852
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1857G>T
  hgvsp: ENST00000389253.4:c.1857G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1845G>T
  hgvsp: ENST00000359692.6:c.1845G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4045G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1857G>T
  hgvsp: ENST00000355667.6:c.1857G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.640G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1857G>T
  hgvsp: ENST00000585892.1:c.1857G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1857G>T
  hgvsp: ENST00000314646.5:c.1857G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3356G>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1845G>T
  hgvsp: ENST00000408974.4:c.1845G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2835
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser619Ser
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

19-10934554-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934554
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934554
    reference: chr 19
allele count: 2
allele frequency: 1.67221283925018e-5
allele num: 119602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4060C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.655C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1860C>T
  hgvsp: ENST00000359692.6:c.1860C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1872C>T
  hgvsp: ENST00000585892.1:c.1872C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3371C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1860C>T
  hgvsp: ENST00000408974.4:c.1860C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1872C>T
  hgvsp: ENST00000314646.5:c.1872C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1872C>T
  hgvsp: ENST00000355667.6:c.1872C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1872C>T
  hgvsp: ENST00000389253.4:c.1872C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly624Gly
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-10934555-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934555
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934555
    reference: chr 19
allele count: 3
allele frequency: 2.508654859264463e-5
allele num: 119586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.656G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3372G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4061G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1873G>A
  hgvsp: ENSP00000468734.1:p.Val625Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1861G>A
  hgvsp: ENSP00000352721.6:p.Val621Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1873G>A
  hgvsp: ENSP00000347890.6:p.Val625Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1873G>A
  hgvsp: ENSP00000313164.5:p.Val625Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1873G>A
  hgvsp: ENSP00000373905.3:p.Val625Ile
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1861G>A
  hgvsp: ENSP00000386192.3:p.Val621Ile
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34789
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9094
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2814
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val625Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

19-10934563-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934563
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934563
    reference: chr 19
allele count: 3
allele frequency: 2.513699663164245e-5
allele num: 119346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.664C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1869C>G
  hgvsp: ENST00000359692.6:c.1869C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1881C>G
  hgvsp: ENST00000585892.1:c.1881C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1881C>G
  hgvsp: ENST00000314646.5:c.1881C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1881C>G
  hgvsp: ENST00000355667.6:c.1881C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1881C>G
  hgvsp: ENST00000389253.4:c.1881C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1869C>G
  hgvsp: ENST00000408974.4:c.1869C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3380C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4069C>G
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23475
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11984
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro627Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

19-10934564-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934564
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934564
    reference: chr 19
allele count: 1
allele frequency: 8.377735330585436e-6
allele num: 119364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4070G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1882G>A
  hgvsp: ENSP00000313164.5:p.Glu628Lys
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1870G>A
  hgvsp: ENSP00000352721.6:p.Glu624Lys
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.665G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1882G>A
  hgvsp: ENSP00000347890.6:p.Glu628Lys
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1870G>A
  hgvsp: ENSP00000386192.3:p.Glu624Lys
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3381G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1882G>A
  hgvsp: ENSP00000373905.3:p.Glu628Lys
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1882G>A
  hgvsp: ENSP00000468734.1:p.Glu628Lys
  variant of: http://identifiers.org/hgnc/2974
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu628Lys
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

19-10934585-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934585
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934585
    reference: chr 19
allele count: 7
allele frequency: 5.954304962487879e-5
allele num: 117562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+10C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+10C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+10C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+10C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3402C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+10C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+10C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+10C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+10C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20829
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9316
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29240
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4760
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-10934586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934586
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934586
    reference: chr 19
allele count: 4
allele frequency: 3.410117819570666e-5
allele num: 117298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3403G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+11G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+11G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+11G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+11G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+11G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+11G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+11G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+11G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20521
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9861
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5879
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1516
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-10934590-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934590
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934590
    reference: chr 19
allele count: 4
allele frequency: 3.422254923769271e-5
allele num: 116882
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3407T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+15T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+15T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+15T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+15T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+15T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+15T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+15T>C
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+15T>C
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9673
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20031
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6985
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1840
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
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: T
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

19-10934592-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934592
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934592
    reference: chr 19
allele count: 12
allele frequency: 1.032222547181172e-4
allele num: 116254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+17C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+17C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+17C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3409C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+17C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+17C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+17C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+17C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+17C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9816
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19533
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8713
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6395
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6454
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24562
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ

19-10934593-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934593
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934593
    reference: chr 19
allele count: 7
allele frequency: 6.026067044300201e-5
allele num: 116162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+18G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+18G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+18G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+18G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+18G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3410G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+18G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+18G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+18G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19551
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5521
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2962
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24940
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

19-10934598-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934598
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934598
    reference: chr 19
allele count: 1
allele frequency: 8.813834194151139e-6
allele num: 113458
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+23C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+23C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+23C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3415C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+23C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+23C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+23C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+23C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+23C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7840
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5194
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6501
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

19-10934606-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934606
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934607
    reference: chr 19
allele count: 8267
allele frequency: 7.182574849258892e-2
allele num: 115098
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+31_1881+32insC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3423_3424insC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+31_1893+32insC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+31_1893+32insC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+31_4081+32insC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+31_1893+32insC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+31_676+32insC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+31_1881+32insC
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+31_1893+32insC
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.75e1
  variant carriers: 196
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 4.25e1
  variant carriers: 364
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 5.25e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 679
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 1.25e1
  variant carriers: 421
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 7.5e0
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 3.25e1
  variant carriers: 1176
genotype depth: GenotypeDepth
  all individuals: 10064
  bin: 2.25e1
  variant carriers: 1572
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 5.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 7339
  bin: 1.75e1
  variant carriers: 1048
genotype depth: GenotypeDepth
  all individuals: 15572
  bin: 2.75e1
  variant carriers: 1537
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.25e1
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 3488
  bin: 3.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 1.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 8.25e1
  variant carriers: 63
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 7.5e0
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.5e0
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 5640
  bin: 2.25e1
  variant carriers: 17
num of homozygotes: 734
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP

19-10934609-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934609
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934609
    reference: chr 19
allele count: 1
allele frequency: 8.760556470547009e-6
allele num: 114148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+34C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3426C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+34C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+34C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+34C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+34C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+34C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+34C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+34C>G
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14848
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6080
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/19-10934612-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934612
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934612
    reference: chr 19
allele count: 2
allele frequency: 1.747335313646689e-5
allele num: 114460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+37C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+37C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3429C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+37C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+37C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+37C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+37C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+37C>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+37C>A
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8846
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8833
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1768
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6692
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1598
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

19-10934613-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934613
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934613
    reference: chr 19
allele count: 6
allele frequency: 5.249711265880376e-5
allele num: 114292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3430C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+38C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+38C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+38C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+38C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+38C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+38C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+38C>G
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+38C>G
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11593
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6639
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17605
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1834
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

19-10934613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934613
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934613
    reference: chr 19
allele count: 1
allele frequency: 8.749518776467294e-6
allele num: 114292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+38C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+38C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+38C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+38C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+38C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3430C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+38C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+38C>T
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+38C>T
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11593
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3140
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6639
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1834
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4483
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

19-10934619-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10934619
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10934619
    reference: chr 19
allele count: 3
allele frequency: 2.64335812215839e-5
allele num: 113492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590787
  gene symbol: DNM2
  hgvsc: ENST00000590787.1:n.3436G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000468734
  ensembl transcript: ENST00000585892
  gene symbol: DNM2
  hgvsc: ENST00000585892.1:c.1893+44G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000593203
  gene symbol: DNM2
  hgvsc: ENST00000593203.1:n.676+44G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl transcript: ENST00000590806
  gene symbol: DNM2
  hgvsc: ENST00000590806.1:n.4081+44G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000352721
  ensembl transcript: ENST00000359692
  gene symbol: DNM2
  hgvsc: ENST00000359692.6:c.1881+44G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000313164
  ensembl transcript: ENST00000314646
  gene symbol: DNM2
  hgvsc: ENST00000314646.5:c.1893+44G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000347890
  ensembl transcript: ENST00000355667
  gene symbol: DNM2
  hgvsc: ENST00000355667.6:c.1893+44G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000386192
  ensembl transcript: ENST00000408974
  gene symbol: DNM2
  hgvsc: ENST00000408974.4:c.1881+44G>A
  variant of: http://identifiers.org/hgnc/2974
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079805
  ensembl protein: ENSP00000373905
  ensembl transcript: ENST00000389253
  gene symbol: DNM2
  hgvsc: ENST00000389253.4:c.1893+44G>A
  variant of: http://identifiers.org/hgnc/2974
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8718
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10231
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13048
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6400
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5524
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6067
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G

GenotypeQuality
all individuals: 325
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5280
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.369112814895947e-4
allele num: 7304
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7442
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

QD
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SIO_000300: 8.960000000000001e0

FS
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SIO_000300: 2.097e0

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

InbreedingCoeff
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SIO_000300: -7.35e-2

VQSLOD
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SIO_000300: -1.619e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-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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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7352
num of homozygotes: 0

African
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allele count: 1
allele frequency: 4.139072847682119e-4
allele num: 2416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 7096
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.16e-1

DP
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VQSLOD
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SIO_000300: -1.573e0

FS
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MQ
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: -7.71e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-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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bin: 7.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 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: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.16617e6

FS
type: SiteQuality
SIO_000300: 2.526e0

VQSLOD
type: SiteQuality
SIO_000300: 3.77e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.599e0

QD
type: SiteQuality
SIO_000300: 1.013e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e-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
all individuals: 20
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variant carriers: 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: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.266e0

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-1

QD
type: SiteQuality
SIO_000300: 1.362e1

DP
type: SiteQuality
SIO_000300: 2.166635e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.199e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.31e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 44

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 40
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variant carriers: 0

GenotypeQuality
all individuals: 2036
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variant carriers: 0

South Asian
type: Population
allele count: 26
allele frequency: 1.574803149606299e-3
allele num: 16510
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

East Asian
type: Population
allele count: 15
allele frequency: 1.734104046242775e-3
allele num: 8650
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

QD
type: SiteQuality
SIO_000300: 1.425e1

DP
type: SiteQuality
SIO_000300: 2.167244e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-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
all individuals: 13243
bin: 9.75e1
variant carriers: 50

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 12
allele frequency: 1.036448436690275e-3
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.885170225043277e-4
allele num: 10398
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: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 35
allele frequency: 5.246432425950354e-4
allele num: 66712
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.16601e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.15e-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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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 16510
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.6e-3

ClippingRankSum
type: SiteQuality
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FS
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QD
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.951e1

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: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 8.992805755395684e-5
allele num: 66720
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
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MQRankSum
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MQ
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SIO_000300: 5.518e1

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

East Asian
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num of homozygotes: 0

South Asian
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Other
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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BaseQRankSum
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MQ
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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bin: 7.75e1
variant carriers: 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: 11578
num of homozygotes: 0

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

South Asian
type: Population
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allele frequency: 6.056935190793458e-5
allele num: 16510
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66722
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African
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ClippingRankSum
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QD
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BaseQRankSum
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MQ
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FS
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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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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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 1.211387038158692e-4
allele num: 16510
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Other
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DP
type: SiteQuality
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FS
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BaseQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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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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variant carriers: 0

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

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

Other
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South Asian
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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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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South Asian
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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MQ
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

South Asian
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num of homozygotes: 0

East Asian
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VQSLOD
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DP
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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MQ
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ClippingRankSum
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QD
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BaseQRankSum
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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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variant carriers: 0

South Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66718
num of homozygotes: 0

African
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European (Finnish)
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Other
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Latino
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East Asian
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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African
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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQ
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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DP
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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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East Asian
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Latino
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European (Finnish)
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Other
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South Asian
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African
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European (Non-Finnish)
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InbreedingCoeff
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BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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MQ
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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Other
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Latino
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South Asian
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European (Finnish)
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DP
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001200480192077e-5
allele num: 66640
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.283e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e-1

QD
type: SiteQuality
SIO_000300: 1.479e1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

MQRankSum
type: SiteQuality
SIO_000300: 4.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 8.0e-1

DP
type: SiteQuality
SIO_000300: 2.161104e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.09e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.434e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.3925e1

DP
type: SiteQuality
SIO_000300: 2.159914e6

QD
type: SiteQuality
SIO_000300: 9.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.662e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 373
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4070
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
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: 1.503126503126503e-5
allele num: 66528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

QD
type: SiteQuality
SIO_000300: 1.536e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.068e0

FS
type: SiteQuality
SIO_000300: 1.658e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

DP
type: SiteQuality
SIO_000300: 2.155277e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.93e-1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 13179
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variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66398
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.371e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.8e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.53e-1

DP
type: SiteQuality
SIO_000300: 2.147127e6

VQSLOD
type: SiteQuality
SIO_000300: -1.949e0

QD
type: SiteQuality
SIO_000300: 1.672e1

GenotypeQuality
all individuals: 19525
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 13185
bin: 9.75e1
variant carriers: 75

GenotypeQuality
all individuals: 3165
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variant carriers: 1

GenotypeQuality
all individuals: 188
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variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
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variant carriers: 0

GenotypeQuality
all individuals: 3616
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variant carriers: 0

GenotypeQuality
all individuals: 8698
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 74
allele frequency: 7.170542635658915e-3
allele num: 10320
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506114826194349e-5
allele num: 66396
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.146959e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

QD
type: SiteQuality
SIO_000300: 1.484e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.592e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

GenotypeQuality
all individuals: 13129
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 3593
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variant carriers: 0

GenotypeQuality
all individuals: 163
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GenotypeQuality
all individuals: 5154
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 97
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GenotypeQuality
all individuals: 19230
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variant carriers: 0

GenotypeQuality
all individuals: 753
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variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.142e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.474e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.526e-1

QD
type: SiteQuality
SIO_000300: 1.379e1

DP
type: SiteQuality
SIO_000300: 2.139513e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

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
all individuals: 13120
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variant carriers: 1

GenotypeQuality
all individuals: 4959
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510254628930438e-5
allele num: 66214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.92e-1

DP
type: SiteQuality
SIO_000300: 2.103298e6

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 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
all individuals: 3987
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variant carriers: 0

GenotypeQuality
all individuals: 4948
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510893542441e-5
allele num: 66186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.132e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

DP
type: SiteQuality
SIO_000300: 2.097754e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.557e0

VQSLOD
type: SiteQuality
SIO_000300: 6.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.23e-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
all individuals: 36
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.024254521260509e-5
allele num: 66132
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.086977e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.498e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.96e-1

BaseQRankSum
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SIO_000300: 3.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.4e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

GenotypeQuality
all individuals: 1465
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variant carriers: 0

GenotypeQuality
all individuals: 802
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variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 5.75e1
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GenotypeQuality
all individuals: 280
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GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 2002
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GenotypeQuality
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GenotypeQuality
all individuals: 7667
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GenotypeQuality
all individuals: 13098
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variant carriers: 2

GenotypeQuality
all individuals: 973
bin: 3.25e1
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GenotypeQuality
all individuals: 3951
bin: 8.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51290508033526e-5
allele num: 66098
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.725734292939116e-5
allele num: 10282
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

QD
type: SiteQuality
SIO_000300: 1.365e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 2.081129e6

FS
type: SiteQuality
SIO_000300: 6.291e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.505e0

GenotypeQuality
all individuals: 1545
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13072
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3189
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15122
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.575757575757576e-5
allele num: 66000
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.351e1

FS
type: SiteQuality
SIO_000300: 9.762e0

MQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.417e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

DP
type: SiteQuality
SIO_000300: 2.044047e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.798e0

GenotypeQuality
all individuals: 2197
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3059
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3106
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 13074
bin: 9.75e1
variant carriers: 36

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.03905181583346e-5
allele num: 65810
num of homozygotes: 0

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

Other
type: Population
allele count: 3
allele frequency: 3.333333333333334e-3
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 33
allele frequency: 2.007299270072993e-3
allele num: 16440
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

QD
type: SiteQuality
SIO_000300: 1.418e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e0

DP
type: SiteQuality
SIO_000300: 2.004171e6

GenotypeQuality
all individuals: 3121
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6230
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 962
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.002803925495694e-4
allele num: 9986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65162
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.879e-1

DP
type: SiteQuality
SIO_000300: 1.871996e6

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.981e1

FS
type: SiteQuality
SIO_000300: 5.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

GenotypeQuality
all individuals: 257
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 308
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 895
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variant carriers: 1

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

GenotypeQuality
all individuals: 217
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variant carriers: 6

GenotypeQuality
all individuals: 400
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variant carriers: 4

GenotypeQuality
all individuals: 273
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variant carriers: 9

GenotypeQuality
all individuals: 244
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variant carriers: 4

GenotypeQuality
all individuals: 2831
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6078
bin: 9.75e1
variant carriers: 24

GenotypeQuality
all individuals: 33147
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 8838
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variant carriers: 1

GenotypeQuality
all individuals: 388
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variant carriers: 9

GenotypeQuality
all individuals: 695
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variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 2.25e1
variant carriers: 9

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

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

European (Non-Finnish)
type: Population
allele count: 61
allele frequency: 9.453260600049591e-4
allele num: 64528
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.11115610447459e-4
allele num: 9878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.737015806843842e-4
allele num: 11514
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.822157434402332e-4
allele num: 16464
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.33e-1

QD
type: SiteQuality
SIO_000300: 2.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.92e-1

DP
type: SiteQuality
SIO_000300: 1.906705e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.64e-1

GenotypeQuality
all individuals: 257
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
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variant carriers: 0

GenotypeQuality
all individuals: 288
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variant carriers: 0

GenotypeQuality
all individuals: 2507
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variant carriers: 0

GenotypeQuality
all individuals: 244
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variant carriers: 0

GenotypeQuality
all individuals: 273
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variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 6078
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 273
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33147
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1579
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8838
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2831
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.198859409868585e-5
allele num: 64528
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.906705e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

FS
type: SiteQuality
SIO_000300: 8.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.92e-1

QD
type: SiteQuality
SIO_000300: 2.68e0

GenotypeQuality
all individuals: 880
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 364
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
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GenotypeQuality
all individuals: 150
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8893
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2503
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2825
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.548658861426005e-5
allele num: 64572
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.189e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.03e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

FS
type: SiteQuality
SIO_000300: 1.452e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.93e-1

DP
type: SiteQuality
SIO_000300: 1.913002e6

VQSLOD
type: SiteQuality
SIO_000300: 3.76e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.341e1

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

GenotypeQuality
all individuals: 369
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33640
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
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GenotypeQuality
all individuals: 237
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
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variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.75e1
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GenotypeQuality
all individuals: 150
bin: 5.25e1
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GenotypeQuality
all individuals: 6256
bin: 9.75e1
variant carriers: 332

GenotypeQuality
all individuals: 2825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8893
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 16
allele frequency: 1.389130057301615e-3
allele num: 11518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.09731772285201e-5
allele num: 64572
num of homozygotes: 0

African
type: Population
allele count: 314
allele frequency: 3.171076550191881e-2
allele num: 9902
num of homozygotes: 4

Other
type: Population
allele count: 4
allele frequency: 4.545454545454545e-3
allele num: 880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.76e0

FS
type: SiteQuality
SIO_000300: 1.452e0

DP
type: SiteQuality
SIO_000300: 1.913002e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.189e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

MQ
type: SiteQuality
SIO_000300: 5.979e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.93e-1

QD
type: SiteQuality
SIO_000300: 1.341e1

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 82
bin: 4.25e1
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GenotypeQuality
all individuals: 683
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variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 2850
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9127
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 3.75e1
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GenotypeQuality
all individuals: 5963
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2562
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10030
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65242
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.32e1

VQSLOD
type: SiteQuality
SIO_000300: 6.929999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.891895e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.671e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

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

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

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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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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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 1028
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2563
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.132523840186429e-5
allele num: 65226
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.24e0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 4.319e0

DP
type: SiteQuality
SIO_000300: 1.892061e6

QD
type: SiteQuality
SIO_000300: 1.186e1

GenotypeQuality
all individuals: 9123
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5966
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2852
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10026
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.066261920093214e-5
allele num: 65226
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.03e-1

QD
type: SiteQuality
SIO_000300: 1.186e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.24e0

FS
type: SiteQuality
SIO_000300: 4.319e0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.29e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 1.892061e6

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
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variant carriers: 28

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 161
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variant carriers: 0

GenotypeQuality
all individuals: 1577
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533083951677194e-5
allele num: 65228
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.332004851845434e-4
allele num: 11542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

African
type: Population
allele count: 21
allele frequency: 2.093718843469591e-3
allele num: 10030
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.362e1

DP
type: SiteQuality
SIO_000300: 1.893381e6

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

GenotypeQuality
all individuals: 1024
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 34707
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variant carriers: 0

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 271
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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: 2545
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GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
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: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.068990915786889e-5
allele num: 65168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

DP
type: SiteQuality
SIO_000300: 1.892466e6

MQ
type: SiteQuality
SIO_000300: 5.941e1

FS
type: SiteQuality
SIO_000300: 1.162e0

MQRankSum
type: SiteQuality
SIO_000300: 4.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.49e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

VQSLOD
type: SiteQuality
SIO_000300: 7.23e-1

GenotypeQuality
all individuals: 168
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 1024
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variant carriers: 0

GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 1575
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 679
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variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 5942
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 878
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9124
bin: 6.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.068990915786889e-5
allele num: 65168
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.126126126126126e-3
allele num: 888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.941e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: 4.69e-1

FS
type: SiteQuality
SIO_000300: 1.162e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.23e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.49e-1

DP
type: SiteQuality
SIO_000300: 1.892466e6

GenotypeQuality
all individuals: 243
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 135
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GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
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GenotypeQuality
all individuals: 115
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GenotypeQuality
all individuals: 2841
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 5939
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2556
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65330
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.946290033817386e-5
allele num: 10054
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.470000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.671e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.703e0

FS
type: SiteQuality
SIO_000300: 8.070000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.032e0

DP
type: SiteQuality
SIO_000300: 1.89361e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e0

GenotypeQuality
all individuals: 1043
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 130
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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: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 879
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65358
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

FS
type: SiteQuality
SIO_000300: 1.99e1

VQSLOD
type: SiteQuality
SIO_000300: -2.691e0

QD
type: SiteQuality
SIO_000300: 1.113e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

DP
type: SiteQuality
SIO_000300: 1.894181e6

MQ
type: SiteQuality
SIO_000300: 5.922e1

GenotypeQuality
all individuals: 878
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 679
bin: 8.75e1
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GenotypeQuality
all individuals: 2566
bin: 7.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528584530724549e-5
allele num: 65420
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-1

DP
type: SiteQuality
SIO_000300: 1.896079e6

FS
type: SiteQuality
SIO_000300: 2.548e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.299e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.64e-1

QD
type: SiteQuality
SIO_000300: 9.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2842
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
type: Population
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allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.528164063693878e-5
allele num: 65438
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
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DP
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: -5.12e-1

FS
type: SiteQuality
SIO_000300: 7.691e0

InbreedingCoeff
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SIO_000300: 1.8e-3

MQ
type: SiteQuality
SIO_000300: 5.934e1

ReadPosRankSum
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SIO_000300: 4.92e-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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bin: 6.25e1
variant carriers: 0

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

Other
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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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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

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

FS
type: SiteQuality
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DP
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QD
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQRankSum
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SIO_000300: 9.82e-1

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -9.23e-1

BaseQRankSum
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SIO_000300: 1.79e0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.523090045083465e-5
allele num: 65656
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
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ReadPosRankSum
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SIO_000300: -3.36e-1

BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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QD
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8602
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65654
num of homozygotes: 0

African
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allele count: 8
allele frequency: 7.855459544383347e-4
allele num: 10184
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

DP
type: SiteQuality
SIO_000300: 1.903331e6

MQ
type: SiteQuality
SIO_000300: 5.953e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.09e-1

FS
type: SiteQuality
SIO_000300: 1.125e0

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

QD
type: SiteQuality
SIO_000300: 1.093e1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

South Asian
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allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.522533495736906e-5
allele num: 65680
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.903487e6

VQSLOD
type: SiteQuality
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MQRankSum
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MQ
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e-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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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
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allele frequency: 2.511257360581919e-3
allele num: 11548
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Other
type: Population
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MQ
type: SiteQuality
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DP
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QD
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6612
num of homozygotes: 0

Other
type: Population
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Latino
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
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allele num: 65680
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South Asian
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African
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MQRankSum
type: SiteQuality
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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MQRankSum
type: SiteQuality
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FS
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DP
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.525180733916969e-5
allele num: 65566
num of homozygotes: 0

Latino
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allele frequency: 2.600104004160167e-4
allele num: 11538
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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FS
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MQ
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VQSLOD
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MQRankSum
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SIO_000300: 7.86e-1

QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.27e-1

GenotypeQuality
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variant carriers: 2

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

Other
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allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.050361467833938e-5
allele num: 65566
num of homozygotes: 0

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

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

MQ
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.057542958478566e-5
allele num: 65412
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.425e0

MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: 9.51e-1

MQRankSum
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QD
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DP
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ClippingRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.28e-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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bin: 9.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.977456990310461e-4
allele num: 10114
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529239050648397e-5
allele num: 65392
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.57e-1

DP
type: SiteQuality
SIO_000300: 1.889699e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.925e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.533460099368214e-5
allele num: 65212
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.523925632429137e-4
allele num: 6562
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.912767644726408e-5
allele num: 10088
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.943e1

FS
type: SiteQuality
SIO_000300: 9.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.281e0

DP
type: SiteQuality
SIO_000300: 1.883182e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

VQSLOD
type: SiteQuality
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QD
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SIO_000300: 1.045e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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allele num: 16488
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.53298994358597e-5
allele num: 65232
num of homozygotes: 0

European (Finnish)
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allele count: 0
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Other
type: Population
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allele frequency: 0.0e0
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
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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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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.756543123133673e-4
allele num: 11386
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.807376409231441e-5
allele num: 64042
num of homozygotes: 0

Other
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6498
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African
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

MQ
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MQRankSum
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FS
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DP
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 4.696158542312388e-5
allele num: 63882
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African
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East Asian
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European (Finnish)
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South Asian
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Latino
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Other
type: Population
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
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num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63648
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.448280083241523e-4
allele num: 16338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.755194e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.204e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.485e0

MQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

GenotypeQuality
all individuals: 557
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2925
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 610
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2435
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5873
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1634
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.104309964031047e-4
allele num: 63388
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.030078285949732e-4
allele num: 9708
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11248
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.838235294117647e-4
allele num: 16320
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.208313194780087e-4
allele num: 8276
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

FS
type: SiteQuality
SIO_000300: 9.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

QD
type: SiteQuality
SIO_000300: 1.356e1

DP
type: SiteQuality
SIO_000300: 1.73032e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 624
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6452
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5867
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1976
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6418
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.156665298778371e-5
allele num: 63358
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.153576582148011e-4
allele num: 9702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8224
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16312
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.793e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

QD
type: SiteQuality
SIO_000300: 1.414e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

FS
type: SiteQuality
SIO_000300: 3.978e0

DP
type: SiteQuality
SIO_000300: 1.727205e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 775
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2395
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3662
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1699
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5847
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 602
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2524
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22501
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.191176470588235e-5
allele num: 10880
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.014e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 1.678048e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.953e1

VQSLOD
type: SiteQuality
SIO_000300: -1.858e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 6.06e1

GenotypeQuality
all individuals: 238
bin: 1.25e1
variant carriers: 11

GenotypeQuality
all individuals: 864
bin: 4.75e1
variant carriers: 36

GenotypeQuality
all individuals: 19131
bin: 6.25e1
variant carriers: 47

GenotypeQuality
all individuals: 555
bin: 5.25e1
variant carriers: 60

GenotypeQuality
all individuals: 369
bin: 5.75e1
variant carriers: 55

GenotypeQuality
all individuals: 967
bin: 4.25e1
variant carriers: 37

GenotypeQuality
all individuals: 2551
bin: 3.75e1
variant carriers: 35

GenotypeQuality
all individuals: 4497
bin: 6.75e1
variant carriers: 59

GenotypeQuality
all individuals: 828
bin: 9.25e1
variant carriers: 45

GenotypeQuality
all individuals: 2403
bin: 2.75e1
variant carriers: 30

GenotypeQuality
all individuals: 1559
bin: 7.25e1
variant carriers: 68

GenotypeQuality
all individuals: 1968
bin: 7.75e1
variant carriers: 38

GenotypeQuality
all individuals: 12540
bin: 9.75e1
variant carriers: 6962

GenotypeQuality
all individuals: 625
bin: 8.75e1
variant carriers: 67

South Asian
type: Population
allele count: 562
allele frequency: 3.461870149069853e-2
allele num: 16234
num of homozygotes: 15

European (Finnish)
type: Population
allele count: 582
allele frequency: 9.056956115779645e-2
allele num: 6426
num of homozygotes: 23

European (Non-Finnish)
type: Population
allele count: 1697
allele frequency: 2.711469018630365e-2
allele num: 62586
num of homozygotes: 21

Other
type: Population
allele count: 56
allele frequency: 6.436781609195402e-2
allele num: 870
num of homozygotes: 6

African
type: Population
allele count: 870
allele frequency: 9.045539613225202e-2
allele num: 9618
num of homozygotes: 40

Latino
type: Population
allele count: 1432
allele frequency: 1.289625360230547e-1
allele num: 11104
num of homozygotes: 86

East Asian
type: Population
allele count: 3068
allele frequency: 3.714285714285714e-1
allele num: 8260
num of homozygotes: 543

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.076e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.14e0

QD
type: SiteQuality
SIO_000300: 1.86e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.627106e6

GenotypeQuality
all individuals: 1333
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4676
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6511
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19639
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2983
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4610
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3641
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.607200257152041e-5
allele num: 62220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.455e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.562163e6

GenotypeQuality
all individuals: 1662
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4257
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5014
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1377
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18242
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6080
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3097
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 716
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4572
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2076
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.215123943028004e-5
allele num: 62206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11108
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.83e-1

DP
type: SiteQuality
SIO_000300: 1.539426e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.61e-1

QD
type: SiteQuality
SIO_000300: 1.118e1

GenotypeQuality
all individuals: 4483
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3140
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4437
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5129
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2046
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1878
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6081
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1356
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8114
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.16827041697508e-5
allele num: 16212
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.127932436659368e-4
allele num: 6394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.832007215797442e-5
allele num: 62086
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.246e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

FS
type: SiteQuality
SIO_000300: 9.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.41e0

DP
type: SiteQuality
SIO_000300: 1.533725e6

GenotypeQuality
all individuals: 5129
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4437
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17605
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1356
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6081
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.16827041697508e-5
allele num: 16212
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: 11086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62086
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8114
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.41e0

QD
type: SiteQuality
SIO_000300: 1.246e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.44e0

FS
type: SiteQuality
SIO_000300: 9.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.533725e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

GenotypeQuality
all individuals: 3305
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2763
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1466
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5512
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13458
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3522
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3924
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 7.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.743448964312453e-4
allele num: 8014
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11006
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16162
num of homozygotes: 0