RS730882035 VHL

Health Risk Chr 3:10149805
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Von Hippel-Lindau syndrome
Chuvash polycythemia
Hereditary cancer-predisposing syndrome
VHL-related disorder
Inherited phaeochromocytoma and paraganglioma excluding NF1
Pheochromocytoma
Nonpapillary renal cell carcinoma
Hereditary cancer-predisposing syndrome
Von Hippel-Lindau syndrome
Chuvash polycythemia
Hereditary cancer-predisposing syndrome
VHL-related disorder
Inherited phaeochromocytoma and paraganglioma excluding NF1
Pheochromocytoma
Nonpapillary renal cell carcinoma
Other Variants in VHL
rs794729660 rs5030823 rs5030821 rs5030818 rs5030820 rs119103277 rs119103278 rs104893824 rs5030809 rs104893825
Ask Dr. Hemsworth about this variant