| | | 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 | |
| | TFAP2E, TFAP2E-AS1 (A107S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TFAP2E, TFAP2E-AS1 (H110Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TFAP2E, TFAP2E-AS1 (A123V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TFAP2E, TFAP2E-AS1 (P137S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TFAP2E, TFAP2E-AS1 (G146S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TFAP2E-AS1, TFAP2E (A161V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TFAP2E, TFAP2E-AS1 (E167G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TFAP2E, TFAP2E-AS1 (E174Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TFAP2E, TFAP2E-AS1 (M177L) | 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 | |