| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | RPL17, RPL17-C18orf32 (M171T +3 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | RPL17-C18orf32, RPL17 (N64S +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene