| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130058878, CTF1 (A92T +1 more) | Single nucleotide variant (missense variant +1 more) | Dilated Cardiomyopathy, Dominant +2 more | GConflicting classifications of pathogenicity |
| | CTF1, LOC130058878 (P115R +1 more) | Indel (missense variant +1 more) | not specified | |
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