RS397514565 PIK3CA
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What This Variant Does
"CLNSIG=5
Associated Conditions
Megalencephaly-capillary malformation-polymicrogyria syndrome
PIK3CA related overgrowth syndrome
Cowden syndrome
PIK3CA-related disorder
Epidermal nevus
Diffuse midline glioma
H3 K27M-mutant
Megalencephaly-capillary malformation-polymicrogyria syndrome
PIK3CA related overgrowth syndrome
Cowden syndrome
PIK3CA-related disorder
Epidermal nevus
Diffuse midline glioma
H3 K27M-mutant
Other Variants in PIK3CA