| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FNIP1, LOC129994555 (D25A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FNIP1, LOC129994555 (A18V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FNIP1, LOC129994555 (G17A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene