| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LAMC3, LOC126860777 (Q550*) | Single nucleotide variant (nonsense) | not provided +1 more | |
| | LAMC3, LOC126860777 (R551W) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LAMC3, LOC126860777 (R551Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LAMC3, LOC126860777 (R563Q) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC126860777, LAMC3 (G567R) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | LAMC3, LOC126860777 (L575M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LAMC3, LOC126860777 (S585Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LAMC3, LOC126860777 (R587S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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