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rs1800783

From SNPedia

Orientationplus
Stabilizedplus
Make rs1800783(A;A)
Make rs1800783(A;T)
Make rs1800783(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position150992309
GeneNOS3
is asnp
is mentioned by
dbSNPrs1800783
ebirs1800783
HLIrs1800783
Exacrs1800783
Varsomers1800783
Maprs1800783
PheGenIrs1800783
hapmaprs1800783
1000 genomesrs1800783
hgdprs1800783
ensemblrs1800783
gopubmedrs1800783
geneviewrs1800783
scholarrs1800783
googlers1800783
pharmgkbrs1800783
gwascentralrs1800783
openSNPrs1800783
23andMers1800783
23andMe allrs1800783
SNP Nexus

SNPshotrs1800783
SNPdbers1800783
MSV3drs1800783
GWAS Ctlgrs1800783
GMAF0.332
Max Magnitude
Note: this SNP should perhaps be best seen as a proxy for rs4496877, a SNP assayed by the Illumina 1M chip. The pairwise r(2) linkage between the two is reported to be 0.96.[PMID 20962522]
? (A;A) (A;T) (T;T) 28

[PMID 19853644] Promoter polymorphisms of the NOS3 gene are associated with hypnotizability-dependent vascular response to nociceptive stimulation

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

[PMID 20962522] Genetic Polymorphisms in Nitric Oxide Synthase 3 Gene and Implications for Kidney Disease: A Meta-Analysis


[PMID 17980690OA-icon.png] Polymorphisms in the endothelial nitric oxide synthase gene and bone density/ultrasound and geometry in humans.


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


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


[PMID 21252862] NOS3 variants, physical activity, and blood pressure in the European Youth Heart Study.


[PMID 21674837OA-icon.png] Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy.


[PMID 23021696] Single-nucleotide polymorphisms in genes involved in placental function and unexplained stillbirth


[PMID 24035903] The -974 C>A (rs3087459) gene polymorphism in the endothelin gene (EDN1) is associated with risk of developing acute coronary syndrome in Mexican patients


[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