RS777751303 NOTCH3

Health Risk Chr 19:15187126
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What This Variant Does
"CLNSIG=4
Associated Conditions
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 1
Myofibromatosis
infantile
2
Lateral meningocele syndrome
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 1
Myofibromatosis
infantile
2
Other Variants in NOTCH3
rs28937321 rs28933696 rs28933697 rs864621964 rs864621965 rs28933698 rs137852641 rs137852642 rs864621966 rs267606915
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