| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | RHD, RSRP1 (N224T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | RHD, RSRP1 (Q262R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene