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rs1137933

From SNPedia

Orientationminus
Stabilizedminus
Make rs1137933(C;C)
Make rs1137933(C;T)
Make rs1137933(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position27778906
GeneNOS2
is asnp
is mentioned by
dbSNPrs1137933
ebirs1137933
HLIrs1137933
Exacrs1137933
Varsomers1137933
Maprs1137933
PheGenIrs1137933
hapmaprs1137933
1000 genomesrs1137933
hgdprs1137933
ensemblrs1137933
gopubmedrs1137933
geneviewrs1137933
scholarrs1137933
googlers1137933
pharmgkbrs1137933
gwascentralrs1137933
openSNPrs1137933
23andMers1137933
23andMe allrs1137933
SNP Nexus

SNPshotrs1137933
SNPdbers1137933
MSV3drs1137933
GWAS Ctlgrs1137933
GMAF0.2039
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19635578] NO role of NOS2A susceptibility polymorphisms in rheumatoid arthritis


[PMID 15726497OA-icon.png] Gene-environment interaction effects on the development of immune responses in the 1st year of life.


[PMID 17601350OA-icon.png] A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.


[PMID 17955236] Influence of the inducible nitric oxide synthase gene (NOS2A) on inflammatory bowel disease susceptibility.


[PMID 18663495OA-icon.png] Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.


[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 19218192OA-icon.png] Genetic risk factors for portopulmonary hypertension in patients with advanced liver disease.


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


[PMID 19309520OA-icon.png] Nitric oxide synthase 2A (NOS2A) polymorphisms are not associated with invasive pneumococcal disease.


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


[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 20401335OA-icon.png] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.


[PMID 24746566] Genetic variants in inducible nitric oxide synthase gene are associated with the risk of radiation-induced lung injury in lung cancer patients receiving definitive thoracic radiation