| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126863330, RBMX (R369C) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC126863330, RBMX (T297A) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC126863330, RBMX (I161S +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene