RS1060500116 PTEN
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What This Variant Does
"rs1060500116, also known as c.176C>
Associated Conditions
PTEN hamartoma tumor syndrome
Hereditary cancer-predisposing syndrome
Cowden syndrome 1
Familial prostate cancer
Macrocephaly-autism syndrome
Glioma susceptibility 2
Familial meningioma
PTEN hamartoma tumor syndrome
PTEN hamartoma tumor syndrome
Hereditary cancer-predisposing syndrome
Cowden syndrome 1
Familial prostate cancer
Macrocephaly-autism syndrome
Glioma susceptibility 2
Familial meningioma
Other Variants in PTEN