| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129930992, RWDD3
+1 more (L9R) | Single nucleotide variant (missense variant +3 more) | Inborn genetic diseases | |
| | TLCD4-RWDD3, RWDD3 (P35H +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | RWDD3, TLCD4-RWDD3 (P58S +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | RWDD3, TLCD4-RWDD3 (S54W +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | RWDD3, TLCD4-RWDD3 (Q74K +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | RWDD3, TLCD4-RWDD3 (T131A +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | RWDD3, TLCD4-RWDD3 (M120V +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | RWDD3, TLCD4-RWDD3 (A136T +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant +3 more) | Inborn genetic diseases | |
Click to view in NCBI Gene