| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FUZ, LOC105372435 (P182S +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130064942, FUZ
+1 more (V159L +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | FUZ, LOC105372435 (L117V +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene