| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LAMA2, LOC126859784 (L2755R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LAMA2, LOC126859784 (I2776V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LAMA2, LOC126859784 (I2776F +1 more) | Single nucleotide variant (missense variant) | Merosin deficient congenital muscular dystrophy +3 more | |
| | LAMA2, LOC126859784 (T2777N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene