RS869312776 PTEN

Health Risk Chr 10:87933167
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What This Variant Does
"CLNSIG=4
Associated Conditions
Cowden syndrome
PTEN hamartoma tumor syndrome
Hereditary cancer-predisposing syndrome
Cowden syndrome
PTEN hamartoma tumor syndrome
Hereditary cancer-predisposing syndrome
Other Variants in PTEN
rs121909218 rs121909219 rs121909220 rs121909221 rs121909222 rs121909223 rs587776666 rs121909224 rs587776667 rs1554898244
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