| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997982 (G38R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997982 (S39T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997982 (G42S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997982 (G42A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997982 (A43P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129997982, GLCCI1 (G44S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997982 (C51G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997982 (C51W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997982 (A52S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997983 (R102L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997983 (S105R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997983 (S107A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997983 (S108R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GLCCI1, LOC129997983 (P111A) | 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 | |