RS886042002 PIK3CA

Health Risk Chr 3:179199148
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What This Variant Does
"CLNSIG=5
Associated Conditions
Megalencephaly-capillary malformation-polymicrogyria syndrome
Cowden syndrome
See cases
Neoplasm
Inborn genetic diseases
Embryonal rhabdomyosarcoma
Megalencephaly-capillary malformation-polymicrogyria syndrome
Cowden syndrome
See cases
Neoplasm
Inborn genetic diseases
Embryonal rhabdomyosarcoma
Other Variants in PIK3CA
rs104886003 rs121913279 rs121913286 rs121913274 rs587776802 rs121913273 rs121913272 rs587776932 rs397514565 rs121913281
Ask Dr. Hemsworth about this variant