ClinVar Genomic variation as it relates to human health
NM_022361.5(POPDC3):c.75C>T (p.Ala25=)
Germline
Classification
(1)
Likely benign
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 | |||
BVES-AS1 | - | - | - | GRCh38 | - | 31 |
POPDC3 | - | - |
GRCh38 GRCh37 |
- | 47 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
POPDC3-related disorder
|
Likely benign (1) |
|
Nov 4, 2021 | RCV003924060.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 19, 2024