| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CTXN1, LOC130063400 (A26V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CTXN1, LOC130063400 (G23S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene