ClinVar Genomic variation as it relates to human health
NM_016938.5(EFEMP2):c.1092G>A (p.Gln364=)
Germline
Classification
(2)
Likely benign
criteria provided, multiple submitters, no conflicts
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 | |||
EFEMP2 | - | - |
GRCh38 GRCh37 |
432 | 516 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Dec 31, 2021 | RCV002654568.2 | |
Likely benign (1) |
|
Nov 4, 2023 | RCV004072010.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024