| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LAMA2, LOC123864065 (Q2043R) | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | LAMA2, LOC123864065 (V2051I) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LAMA2, LOC123864065 (Q2054R) | Single nucleotide variant (missense variant) | LAMA2-related muscular dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Muscular dystrophy, limb-girdle, autosomal recessive 23 +6 more | |
Click to view in NCBI Gene