| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LANCL2, LOC129998459 (P29L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LANCL2, LOC129998459 (Y31C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LANCL2, LOC129998459 (A35P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LANCL2, LOC129998459 (S41F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LANCL2, LOC129998459 (A44V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LANCL2, LOC129998459 (H64Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LANCL2, LOC129998459 (H64Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |