| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | AIG1, LOC126859817 (I215T +8 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | AIG1, LOC126859817 (C164Y +10 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene