| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FGF19, LOC124500681 (G205R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC124500681, FGF19 (G205R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FGF19, LOC124500681 (E184K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FGF19, LOC124500681 (L179F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC124500681, FGF19 (R140H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FGF19, LOC124500681 (E123K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FGF19, LOC124500681 (S116W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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