ClinVar Genomic variation as it relates to human health
NM_001256071.3(RNF213):c.7656G>A (p.Thr2552=)
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 | |||
RNF213 | - | - |
GRCh38 GRCh37 |
425 | 736 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
RNF213-related disorder
|
Likely benign (1) |
|
Mar 25, 2019 | RCV003944094.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 08, 2024