| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FGF22, LOC130062836 (A15T) | Single nucleotide variant (missense variant) | not specified | |
| | FGF22, LOC130062836 (P34S) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | FGF22, LOC130062836 (L12V) | Single nucleotide variant (missense variant) | not specified | |
| | FGF22, LOC130062836 (P18L) | Single nucleotide variant (missense variant) | not specified | |
Click to view in NCBI Gene