RS753170185 NOTCH3

Health Risk Chr 19:15161009
Upload your DNA to see your genotype for this variant.
Associated Conditions
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 1
Myofibromatosis
infantile
2
Lateral meningocele syndrome
Inborn genetic diseases
NOTCH3-related disorder
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 1
Myofibromatosis
Other Variants in NOTCH3
rs28937321 rs28933696 rs28933697 rs864621964 rs864621965 rs28933698 rs137852641 rs137852642 rs864621966 rs267606915
Ask Dr. Hemsworth about this variant