RS1057519942 PIK3CA

Health Risk Chr 3:179203760
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What This Variant Does
"CLNSIG=4
Associated Conditions
Cowden syndrome
Cowden syndrome 5
Megalencephaly
autosomal dominant
Intestinal duplication
Abnormality of the hairline
Hypertelorism
Diaphragmatic eventration
PIK3CA related overgrowth syndrome
Inborn genetic diseases
Cowden syndrome
Cowden syndrome 5
Megalencephaly
autosomal dominant
Intestinal duplication
Other Variants in PIK3CA
rs104886003 rs121913279 rs121913286 rs121913274 rs587776802 rs121913273 rs121913272 rs587776932 rs397514565 rs121913281
Ask Dr. Hemsworth about this variant