RS121913289 PTEN

Health Risk Chr 10:87958012 delins frameshift variant
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What This Variant Does
"CLNSIG=5
Associated Conditions
PTEN hamartoma tumor syndrome
Hereditary cancer-predisposing syndrome
Malignant lymphoma
large B-cell
diffuse
Cowden syndrome 1
Hereditary cancer-predisposing syndrome
Cowden syndrome 1
Neoplasm
PTEN hamartoma tumor syndrome
Cowden syndrome 1
PTEN hamartoma tumor syndrome
Hereditary cancer-predisposing syndrome
Malignant lymphoma
large B-cell
Population Frequencies
gnomAD ALL
0%
Other Variants in PTEN
rs121909218 rs121909219 rs121909220 rs121909221 rs121909222 rs121909223 rs587776666 rs121909224 rs587776667 rs1554898244
Ask Dr. Hemsworth about this variant