Tag

Cerebrovascular

19 genetic variants with this tag.

RSID	Gene	Description	Category
rs10033464	KCNN3 KCNN3 AF susceptibility variant	Intergenic 4q25 variant near KCNN3 and PITX2 that confers an independent risk...	Arrhythmia & Heart Rhythm	Cerebrovascular	Strong
rs10181656	STAT4	Intronic STAT4 tagging SNP on the primary SLE risk haplotype; the sentinel va...	Interferon Signaling & Systemic Autoimmune	Cerebrovascular	Strong
rs10509679	CYP2C9	Intronic CYP2C9 haplotype tag associated with increased ischemic stroke risk ...	Coronary Artery Disease & Atherosclerosis	Cerebrovascular	Emerging
rs10507391	ALOX5AP SG13S114 intron variant	Intronic ALOX5AP variant in the HapA haplotype; the A allele is associated wi...	Vascular Inflammation & Remodeling	Cerebrovascular	Moderate
rs10958409	SOX17	Intergenic variant near SOX17 at 8q11 that reduces expression of this endothe...	Vascular Inflammation & Remodeling	Cerebrovascular	Strong
rs1333040	CDKN2B-AS1	9p21 locus variant in the ANRIL long non-coding RNA gene associated with intr...	Coronary Artery Disease & Atherosclerosis	Cerebrovascular	Strong
rs4149338	ABCA1 ABCA1 3'UTR Stroke-Associated Variant	3'UTR variant in the ATP-binding cassette transporter A1 gene; the G allele (...	Atherogenic Lipoproteins	Cerebrovascular	Emerging
rs2317676	ITGB3	3' UTR variant in the platelet glycoprotein IIIa gene (ITGB3/GPIIIa) that dis...	Von Willebrand & Anticoagulant Proteins	Cerebrovascular	Moderate
rs17222842	ALOX5AP ALOX5AP variant (SG13S32)	Intronic ALOX5AP haplotype tag; the common G allele marks the HapB cardiovasc...	Vascular Inflammation & Remodeling	Cerebrovascular	Moderate
rs17576	MMP9 MMP9 Q279R	Missense variant in the MMP9 fibronectin type II domain affecting matrix meta...	Coronary Artery Disease & Atherosclerosis	Cerebrovascular	Moderate
rs12598836	HMOX2	Intronic variant near heme oxygenase 2 (HMOX2) associated with migraine-with-...	Neurology & Cognition	Cerebrovascular	Moderate
rs6841581	EDNRA	Regulatory variant upstream of the endothelin receptor type A gene that reduc...	Blood Pressure & Hypertension	Cerebrovascular	Strong
rs3918242	MMP9 MMP9 C-1562T	Promoter variant that disrupts an SP1 transcription factor binding site, incr...	Coronary Artery Disease & Atherosclerosis	Cerebrovascular	Strong
rs17857135	RNF213 Met270Thr	Missense variant (Met270Thr) in RNF213, the major moyamoya disease susceptibi...	Neurology & Cognition	Cerebrovascular	Strong
rs619203	ROS1 Ser2229Cys	Missense variant in the ROS1 receptor tyrosine kinase associated with atherot...	Coronary Artery Disease & Atherosclerosis	Cerebrovascular	Emerging
rs6797312	SERPINI1	Intronic variant in the neuroserpin gene; the A allele has been associated wi...	Coronary Artery Disease & Atherosclerosis	Cerebrovascular	Emerging
rs700651	BOLL	Intronic variant near the BOLL gene associated with increased intracranial an...	Coronary Artery Disease & Atherosclerosis	Cerebrovascular	Moderate
rs767603	LOC105378189	Regulatory variant near LOC105378189 non-coding RNA locus on chromosome 14q23...	Coronary Artery Disease & Atherosclerosis	Cerebrovascular	Moderate
rs9298506	SOX17	Regulatory tag variant near SOX17 at chromosome 8q11.23 associated with intra...	Vascular Inflammation & Remodeling	Cerebrovascular	Strong