| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Deletion (frameshift variant) | Dilated cardiomyopathy 1D | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant +1 more) | Dilated cardiomyopathy 1D | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Indel | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1D | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy | |
| | | Deletion (intron variant +1 more) | not provided | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy, familial restrictive, 3 +2 more | |
| | | Single nucleotide variant (missense variant) | Hypokinetic non-dilated cardiomyopathy | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1DD | |
| | | Single nucleotide variant (missense variant) | not provided | |
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