RS121913381 CDKN2A

Health Risk Chr 9:21971036 snv missense variant
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Familial melanoma
Familial melanoma
Hereditary cancer-predisposing syndrome
Hereditary cancer-predisposing syndrome
Familial melanoma
Familial melanoma
Hereditary cancer-predisposing syndrome
Population Frequencies
gnomAD ALL
100%
Other Variants in CDKN2A
rs121913388 rs587776716 rs104894094 rs1563902635 rs104894095 rs104894097 rs137854598 rs104894098 rs104894099 rs387906410
Ask Dr. Hemsworth about this variant