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rs1800779

From SNPedia

Orientationplus
Stabilizedplus
Make rs1800779(A;A)
Make rs1800779(A;G)
Make rs1800779(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position150992855
GeneNOS3
is asnp
is mentioned by
dbSNPrs1800779
ebirs1800779
HLIrs1800779
Exacrs1800779
Varsomers1800779
Maprs1800779
PheGenIrs1800779
hapmaprs1800779
1000 genomesrs1800779
hgdprs1800779
ensemblrs1800779
gopubmedrs1800779
geneviewrs1800779
scholarrs1800779
googlers1800779
pharmgkbrs1800779
gwascentralrs1800779
openSNPrs1800779
23andMers1800779
23andMe allrs1800779
SNP Nexus

SNPshotrs1800779
SNPdbers1800779
MSV3drs1800779
GWAS Ctlgrs1800779
GMAF0.2502
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19815736OA-icon.png] The Relation between Endothelial Nitric Oxide Synthase Gene Variants and Primary Open-Angle Glaucoma: Interactions with Gender and Postmenopausal Hormone Use



[PMID 20409549] NOS3 gene polymorphisms are associated with risk markers of cardiovascular disease, and interact with omega-3 polyunsaturated fatty acids

[PMID 21122033] Leukoaraiosis is associated with genes regulating blood-brain barrier homeostasis in ischaemic stroke patients


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


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


[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 18246059OA-icon.png] Habitual energy expenditure modifies the association between NOS3 gene polymorphisms and blood pressure.


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


[PMID 18687083] Lack of association of endothelial nitric oxide synthase polymorphisms and migraine.


[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 19493349OA-icon.png] 118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.


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


[PMID 19584173OA-icon.png] Kininogen gene (KNG) variation has a consistent effect on aldosterone response to antihypertensive drug therapy: the GERA 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 21674837OA-icon.png] Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy.


GET Evidence
rs1800779
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.75
summary



[PMID 24192154OA-icon.png] Nitric oxide synthase polymorphisms, gene expression and lung function in chronic obstructive pulmonary disease


[PMID 23826716] Association analysis of nitric oxide synthases: NOS1, NOS2A and NOS3 genes, with multiple sclerosis.


[PMID 25140814OA-icon.png] Association of NOS3 gene variants and clinical contributors of hypoxic-ischemic encephalopathy