RS201680145 NOTCH3

Health Risk Chr 19:15179052
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 1
NOTCH3-related disorder
Cerebral arteriopathy
autosomal dominant
with subcortical infarcts and leukoencephalopathy
type 1
NOTCH3-related disorder
GWAS Studies (3)
Trait Risk Allele OR / Beta P-value Study
Stroke — OR: 2.3 8E-10 PubMed
Subcortical intracerebral hemorrhage — OR: 3.39 4E-9 PubMed
Intracerebral hemorrhage stroke — OR: 3.17 2E-8 PubMed
Other Variants in NOTCH3
rs28937321 rs28933696 rs28933697 rs864621964 rs864621965 rs28933698 rs137852641 rs137852642 rs864621966 rs267606915
Ask Dr. Hemsworth about this variant