| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant +1 more) | Dilated cardiomyopathy 1G +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +1 more) | Dilated cardiomyopathy 1G | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
Click to view in NCBI Gene