ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q25.2-25.3(chr15:84931022-85728834)x1
Germline
Classification
(1)
Likely benign
no assertion criteria provided
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 | |||
ZNF592 | No evidence available | No evidence available |
GRCh38 GRCh37 |
103 | 157 | |
ALPK3 | - | - |
GRCh38 GRCh37 |
2295 | 2423 | |
NMB | - | - |
GRCh38 GRCh38 GRCh37 |
10 | 64 | |
PDE8A | - | - |
GRCh38 GRCh37 |
40 | 96 | |
SEC11A | - | - |
GRCh38 GRCh37 |
6 | 60 | |
SLC28A1 | - | - |
GRCh38 GRCh37 |
67 | 123 | |
WDR73 | - | - |
GRCh38 GRCh38 GRCh37 |
188 | 242 | |
ZSCAN2 | - | - | - |
GRCh38 GRCh38 GRCh37 |
39 | 112 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
- | RCV000521465.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Nov 29, 2022