RS768966657 CDKN2A

Health Risk Chr 9:21971021
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What This Variant Does
"rs768966657, also known as c.335_337dupGTC, p.Arg112_Leu113insArg and Argdup112, represents a mutati...
Associated Conditions
Hereditary cancer-predisposing syndrome
Familial melanoma
Melanoma and neural system tumor syndrome
Hereditary cancer-predisposing syndrome
Familial melanoma
Melanoma and neural system tumor syndrome
Other Variants in CDKN2A
rs121913388 rs587776716 rs104894094 rs1563902635 rs104894095 rs104894097 rs137854598 rs104894098 rs104894099 rs387906410
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