| | PROSER2, PROSER2-AS1 (S34N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (I108V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (G118R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (T146I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2-AS1, PROSER2 (P180A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (R221W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2-AS1, PROSER2 (P228S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (N256S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (R265Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2-AS1, PROSER2 (R265P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (V276A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (Q279R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (R282W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2-AS1, PROSER2 (S311F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2-AS1, PROSER2 (S312F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (P323S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (G324R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (E327G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (L329F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (A331T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (G332R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2-AS1, PROSER2 (R337W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2-AS1, PROSER2 (G338C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (P339S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (P339R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (H349Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (A351S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2-AS1, PROSER2 (L352P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (A373S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (R378W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (R380S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (P386S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (R387W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2-AS1, PROSER2 (A392G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2, PROSER2-AS1 (E433G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PROSER2-AS1, PROSER2 (S435T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |