RS137852642 NOTCH3

Health Risk Chr 19:15192242
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 1
Recurrent subcortical infarcts
Lateral meningocele syndrome
Myofibromatosis
infantile
2
NOTCH3-related disorder
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 1
Recurrent subcortical infarcts
Other Variants in NOTCH3
rs28937321 rs28933696 rs28933697 rs864621964 rs864621965 rs28933698 rs137852641 rs864621966 rs267606915 rs367543285
Ask Dr. Hemsworth about this variant