| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Dilated Cardiomyopathy, Dominant +4 more | |
| | FLNC, LOC129999273 (A709T) | Single nucleotide variant (missense variant) | Dilated Cardiomyopathy, Dominant +6 more | |
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