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rs3918226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs3918226(C;T)
Make rs3918226(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position150993088
GeneNOS3
is asnp
is mentioned by
dbSNPrs3918226
ebirs3918226
HLIrs3918226
Exacrs3918226
Varsomers3918226
Maprs3918226
PheGenIrs3918226
hapmaprs3918226
1000 genomesrs3918226
hgdprs3918226
ensemblrs3918226
gopubmedrs3918226
geneviewrs3918226
scholarrs3918226
googlers3918226
pharmgkbrs3918226
gwascentralrs3918226
openSNPrs3918226
23andMers3918226
23andMe allrs3918226
SNP Nexus

SNPshotrs3918226
SNPdbers3918226
MSV3drs3918226
GWAS Ctlgrs3918226
GMAF0.04316
Max Magnitude0

[PMID 19559392OA-icon.png] A candidate gene association study of 77 polymorphisms in migraine


[PMID 21291465] The association of genetic polymorphisms with cerebral palsy: a meta-analysis

[PMID 17367796OA-icon.png] Association of polymorphisms in NOS3 with the ankle-brachial index in hypertensive adults.

[PMID 18069999] Renin-angiotensin and endothelial nitric oxide synthase gene polymorphisms are not associated with the risk of incident type 2 diabetes mellitus: a prospective cohort study.

[PMID 18513389OA-icon.png] New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.

[PMID 18698212OA-icon.png] Association of renin-angiotensin and endothelial nitric oxide synthase gene polymorphisms with blood pressure progression and incident hypertension: prospective cohort study.

[PMID 19131662OA-icon.png] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.

[PMID 19263529OA-icon.png] Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.

[PMID 19330901OA-icon.png] Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.

[PMID 19619703OA-icon.png] Association of genetic variants with the metabolic syndrome in 20,806 white women: The Women's Health Genome Study.

[PMID 20031567OA-icon.png] An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study.

[PMID 21332392] Endothelial nitric oxide synthase haplotypes associated with aura in patients with migraine.

[PMID 22184326OA-icon.png] Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase.

[PMID 22388798OA-icon.png] Gene panels to help identify subgroups at high and low risk of coronary heart disease among those randomized to antihypertensive treatment: the GenHAT study.

[PMID 22547447] Endothelial nitric oxide synthase polymorphism rs3918226 associated with hypertension does not affect plasma nitrite levels in healthy subjects.


[PMID 22865486] Interaction among nitric oxide (NO)-related genes in migraine susceptibility.