| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126805765, NEXN (R127C +1 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +4 more | |
| | | Microsatellite (inframe_deletion) | Hypertrophic cardiomyopathy 20 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene