RS193922610 VHL

Health Risk Chr 3:10146544
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Von Hippel-Lindau syndrome
Chuvash polycythemia
Hereditary pheochromocytoma and paraganglioma
Nonpapillary renal cell carcinoma
Pheochromocytoma
Hereditary cancer-predisposing syndrome
Von Hippel-Lindau syndrome
Chuvash polycythemia
Hereditary pheochromocytoma and paraganglioma
Nonpapillary renal cell carcinoma
Pheochromocytoma
Other Variants in VHL
rs794729660 rs5030823 rs5030821 rs5030818 rs5030820 rs119103277 rs119103278 rs104893824 rs5030809 rs104893825
Ask Dr. Hemsworth about this variant