| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Duplication (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy +6 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2L +3 more | |
| | | Single nucleotide variant (missense variant) | Miyoshi muscular dystrophy 3 +8 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene