RS786201041 PTEN
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Cowden syndrome 1
PTEN hamartoma tumor syndrome
Diffuse glioma
H3 G34 mutant
Uterine corpus endometrial carcinoma
Melanoma
Cowden syndrome 1
Hereditary cancer-predisposing syndrome
PTEN hamartoma tumor syndrome
Melanoma
PTEN hamartoma tumor syndrome
Cowden syndrome 1
Hereditary cancer-predisposing syndrome
Hereditary cancer-predisposing syndrome
Other Variants in PTEN