RS104894097 CDKN2A

Health Risk Chr 9:21974757
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What This Variant Does
"rs104894097, also known as c.71G&gt
Associated Conditions
Melanoma
cutaneous malignant
susceptibility to
2
Hereditary cancer-predisposing syndrome
Familial melanoma
Melanoma-pancreatic cancer syndrome
Melanoma and neural system tumor syndrome
Familial melanoma
Hereditary cancer-predisposing syndrome
Hereditary cancer
Melanoma
cutaneous malignant
susceptibility to
2
Other Variants in CDKN2A
rs121913388 rs587776716 rs104894094 rs1563902635 rs104894095 rs137854598 rs104894098 rs104894099 rs387906410 rs104894109
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