| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | C2orf49, FHL2 (C275G +2 more) | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy | |
| | FHL2, C2orf49 (C272Y +2 more) | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +1 more | |
| | C2orf49, FHL2 (F239V +2 more) | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy | |
| | FHL2, C2orf49 (K114E +1 more) | Single nucleotide variant (missense variant +1 more) | Primary familial hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
Click to view in NCBI Gene