| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 26 | |
| | | Deletion (frameshift variant) | Hypertrophic cardiomyopathy 26 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 26 +3 more | |
| | | Single nucleotide variant (missense variant) | Myofibrillar myopathy 5 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Myofibrillar myopathy 5 +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Deletion | Hypertrophic cardiomyopathy 26 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 26 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated Cardiomyopathy, Dominant +3 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 26 | |
| | FLNC, FLNC-AS1 (T2386M +1 more) | Single nucleotide variant (missense variant) | Cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | FLNC, FLNC-AS1 (R2641W +1 more) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 26 +3 more | |
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