ClinVar Genomic variation as it relates to human health
GRCh37/hg19 13q13.1-21.31(chr13:32946120-62698217)
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
BRCA2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
18935 | 19094 | |
NBEA | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
506 | 588 | |
RB1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
3622 | 3781 | |
CBY2 | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
43 | 98 | |
AKAP11 | - | - |
GRCh38 GRCh37 |
111 | 169 | |
ALG11 | - | - |
GRCh38 GRCh37 |
77 | 281 | |
ALG5 | - | - |
GRCh38 GRCh37 |
28 | 82 | |
ARL11 | - | - |
GRCh38 GRCh37 |
17 | 86 | |
ATP7B | - | - |
GRCh38 GRCh37 |
2893 | 3035 | |
CAB39L | - | - |
GRCh38 GRCh37 |
22 | 87 |
There are 119 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Mar 1, 2022 | RCV002053048.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 01, 2024