| | | 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 | |
| | LOC126861504, SLC2A13 (L259F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861504, SLC2A13 (A249G) | 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 | |
| | LOC130007683, SLC2A13 (A56V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130007683, SLC2A13 (S53G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130007683, SLC2A13 (T49A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130007684, SLC2A13 (R25S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |