| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | RIC1, LOC126860568 (Q653K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860568, RIC1 (I654M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860568, RIC1 (R721C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860568, RIC1 (R808S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene