| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (R106W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (D107Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (D107E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (S130N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (T141K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (K197N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (N205S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (L210R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (V238I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (V238G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (T246R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (E252Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (L266P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PRAMEF2, LOC126805622 (I277M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (T278I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805622, PRAMEF2 (T278N) | 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 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |