RS193922608 VHL
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What This Variant Does
"Genetic mutation screening in an italian cohort of nonsyndromic pheochromocytoma/paraganglioma patie...
Associated Conditions
Von Hippel-Lindau syndrome
Hereditary cancer-predisposing syndrome
Chuvash polycythemia
Inherited phaeochromocytoma and paraganglioma excluding NF1
Von Hippel-Lindau syndrome
Chuvash polycythemia
Hereditary cancer-predisposing syndrome
Von Hippel-Lindau syndrome
Hereditary cancer-predisposing syndrome
Chuvash polycythemia
Inherited phaeochromocytoma and paraganglioma excluding NF1
Von Hippel-Lindau syndrome
Chuvash polycythemia
Hereditary cancer-predisposing syndrome
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Bullous pemphigoid | — | OR: 2.82 | 9E-38 | PubMed |
Other Variants in VHL