RS754815179 NOTCH3

Health Risk Chr 19:15185344
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Associated Conditions
Inborn genetic diseases
Myofibromatosis
infantile
2
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 1
Lateral meningocele syndrome
Inborn genetic diseases
Myofibromatosis
infantile
2
Cerebral arteriopathy
autosomal dominant
Other Variants in NOTCH3
rs28937321 rs28933696 rs28933697 rs864621964 rs864621965 rs28933698 rs137852641 rs137852642 rs864621966 rs267606915
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