| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | not provided +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Chuvash polycythemia +3 more | |
| | | Single nucleotide variant (intron variant) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | LOC107303340, VHL (R161Q +1 more) | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | LOC107303340, VHL (L198P +1 more) | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
Click to view in NCBI Gene