RS1060500126 PTEN

Health Risk Chr 10:87933223
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What This Variant Does
"CLNSIG=4
Associated Conditions
PTEN hamartoma tumor syndrome
Cowden syndrome 1
Hereditary cancer-predisposing syndrome
PTEN hamartoma tumor syndromes
Gastric cancer
Macrocephaly-autism syndrome
Papillary tumor of the pineal region
Glioma susceptibility 2
Cowden syndrome
Cowden syndrome 1
PTEN hamartoma tumor syndrome
Cowden syndrome 1
Hereditary cancer-predisposing syndrome
PTEN hamartoma tumor syndromes
Gastric cancer
Other Variants in PTEN
rs121909218 rs121909219 rs121909220 rs121909221 rs121909222 rs121909223 rs587776666 rs121909224 rs587776667 rs1554898244
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