RS587782345 PTEN

Health Risk Chr 10:87965326
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
PTEN hamartoma tumor syndrome
Glioma susceptibility 2
Hereditary cancer-predisposing syndrome
PTEN hamartoma tumor syndrome
Glioma susceptibility 2
Other Variants in PTEN
rs121909218 rs121909219 rs121909220 rs121909221 rs121909222 rs121909223 rs587776666 rs121909224 rs587776667 rs1554898244
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