| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | FLNC-related disorder +6 more | GConflicting classifications of pathogenicity |
| | FLNC, FLNC-AS1 (D2394H +1 more) | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene