| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FLNC, FLNC-AS1 (A1889T +1 more) | Inversion (missense variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | FLNC, FLNC-AS1 (R2190C +1 more) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 26 +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | FLNC, FLNC-AS1 (V2264L +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNC, FLNC-AS1 (R2364C +1 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | GConflicting classifications of pathogenicity |
| | FLNC, FLNC-AS1 (G2370S +1 more) | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | FLNC, FLNC-AS1 (R2495H +1 more) | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | FLNC, FLNC-AS1 (V2496A +1 more) | Single nucleotide variant (missense variant) | Myofibrillar myopathy 5 +4 more | |
| | FLNC, FLNC-AS1 (V2581M +1 more) | Single nucleotide variant (missense variant) | Dilated Cardiomyopathy, Dominant +5 more | |
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