| | | 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 | |
| | LOC130005860, TAF6L +1 more (S399N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130005860, TAF6L +1 more (A130G +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130005860, TAF6L +1 more (G409D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TAF6L, TMEM223 (A462S +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130005861, TAF6L +1 more (R503W) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130005861, TAF6L +1 more (A513S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | TMEM223, LOC130005861 +1 more (S519P) | Single nucleotide variant (missense variant +1 more) | 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 | |