| | GALNT10, LOC129995072 (A45G) | 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 | |
| | GALNT10, SAP30L-AS1 (V453M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GALNT10, SAP30L-AS1 (R490P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GALNT10, SAP30L-AS1 (R492H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GALNT10, SAP30L-AS1 (R512Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GALNT10, SAP30L-AS1 (A526T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GALNT10, SAP30L-AS1 (H557Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | SAP30L-AS1, GALNT10 (T592A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | SAP30L-AS1, GALNT10 (N601S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |