| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129998700, SSC4D +1 more (G233E) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ZP3, LOC129998700 +1 more (A224G) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene