| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ANK3, LOC130003862 (H2274R) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | ANK3, LOC130003862 (V2273F) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ANK3, LOC130003862 (A2263E) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ANK3, LOC130003862 (G2259S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene