RS121913293 PTEN
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
PTEN hamartoma tumor syndrome
Cowden syndrome 1
Macrocephaly-autism syndrome
VACTERL with hydrocephalus
Neurodevelopmental delay
Glioma susceptibility 2
Prostate cancer
Familial meningioma
Malignant lymphoma
large B-cell
diffuse
Neoplasm
Diffuse pediatric-type high-grade glioma
H3-wildtype and IDH-wildtype
Other Variants in PTEN