| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CHN1, LOC126806410 (R73W +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | CHN1, LOC126806410 (D77N +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene