RS1060500122 PTEN
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What This Variant Does
"CLNSIG=5
Associated Conditions
PTEN hamartoma tumor syndrome
Hereditary cancer-predisposing syndrome
Cowden syndrome 1
Glioma
PTEN hamartoma tumor syndrome
Hereditary cancer-predisposing syndrome
Cowden syndrome 1
Glioma
Other Variants in PTEN