RS786201044 PTEN

Health Risk Chr 10:87933165
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Acute megakaryoblastic leukemia
Mediastinal germ cell tumor
PTEN hamartoma tumor syndrome
Cowden syndrome
Ovarian neoplasm
Cowden syndrome 1
Glioma susceptibility 2
Glioma
Neoplasm
Hereditary cancer-predisposing syndrome
Acute megakaryoblastic leukemia
Mediastinal germ cell tumor
PTEN hamartoma tumor syndrome
Cowden syndrome
Other Variants in PTEN
rs121909218 rs121909219 rs121909220 rs121909221 rs121909222 rs121909223 rs587776666 rs121909224 rs587776667 rs1554898244
Ask Dr. Hemsworth about this variant