| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (intron variant) | Myofibrillar myopathy 4 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | Myofibrillar myopathy 4 +1 more | |
| | LDB3, LOC110121486 (D117N +1 more) | Single nucleotide variant (missense variant +1 more) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Left ventricular noncompaction cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Myofibrillar myopathy 4 +2 more | |
Click to view in NCBI Gene