RS786204873 PTEN

Health Risk Chr 10:87958020
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What This Variant Does
"CLNSIG=5
Associated Conditions
PTEN hamartoma tumor syndrome
Cowden syndrome 1
Hereditary cancer-predisposing syndrome
Hereditary cancer-predisposing syndrome
PTEN hamartoma tumor syndrome
Squamous cell lung carcinoma
PTEN hamartoma tumor syndrome
PTEN hamartoma tumor syndrome
Cowden syndrome 1
Hereditary cancer-predisposing syndrome
Hereditary cancer-predisposing syndrome
PTEN hamartoma tumor syndrome
Squamous cell lung carcinoma
PTEN hamartoma tumor syndrome
Other Variants in PTEN
rs121909218 rs121909219 rs121909220 rs121909221 rs121909222 rs121909223 rs587776666 rs121909224 rs587776667 rs1554898244
Ask Dr. Hemsworth about this variant