| | EXD2, GALNT16-AS1 (L380P +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (N229S +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (R448C +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (P276L +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (N74Y +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (A211T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (I618V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (G301A +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (Q393R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (R101H +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (P319R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (S455G +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (E406K +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (F612V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (A383T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (E417A +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (C18Y +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (R137H +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (R485W +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | GALNT16-AS1, EXD2 (S263C +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (S275G +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (I259T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EXD2, GALNT16-AS1 (L210F +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |