RS864321640 VHL

Health Risk Chr 3:10149909
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What This Variant Does
"CLNSIG=4
Associated Conditions
Pheochromocytoma
Hereditary cancer-predisposing syndrome
Pheochromocytoma
Hereditary cancer-predisposing syndrome
Other Variants in VHL
rs794729660 rs5030823 rs5030821 rs5030818 rs5030820 rs119103277 rs119103278 rs104893824 rs5030809 rs104893825
Ask Dr. Hemsworth about this variant