| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +9 more | |
| | RNF213, RNF213-AS1 (K3887E) | Single nucleotide variant (missense variant) | Patent foramen ovale +6 more | |
Click to view in NCBI Gene