| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LAMA2, LOC126859784 (L2755P +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LAMA2, LOC126859784 (T2777N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LAMA2, LOC126859784 (R2782C +1 more) | Single nucleotide variant (missense variant) | LAMA2-related muscular dystrophy +1 more | |
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