| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC107303340, VHL (E186D +1 more) | Single nucleotide variant (missense variant +1 more) | Von Hippel-Lindau syndrome +2 more | |
| | LOC107303340, VHL (R200W +1 more) | Single nucleotide variant (missense variant +1 more) | Chuvash polycythemia +6 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene