rs4496877
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | |
(G;T) | 1.1 | For type-1 diabetics, 1.3x increased nephropathy risk |
(T;T) | 1.2 | For type-1 diabetics, 1.6x increased nephropathy risk |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 150983418 |
Gene | NOS3 |
is a | snp |
is | mentioned by |
dbSNP | rs4496877 |
dbSNP (classic) | rs4496877 |
ClinGen | rs4496877 |
ebi | rs4496877 |
HLI | rs4496877 |
Exac | rs4496877 |
Gnomad | rs4496877 |
Varsome | rs4496877 |
LitVar | rs4496877 |
Map | rs4496877 |
PheGenI | rs4496877 |
Biobank | rs4496877 |
1000 genomes | rs4496877 |
hgdp | rs4496877 |
ensembl | rs4496877 |
geneview | rs4496877 |
scholar | rs4496877 |
rs4496877 | |
pharmgkb | rs4496877 |
gwascentral | rs4496877 |
openSNP | rs4496877 |
23andMe | rs4496877 |
SNPshot | rs4496877 |
SNPdbe | rs4496877 |
MSV3d | rs4496877 |
GWAS Ctlg | rs4496877 |
GMAF | 0.2199 |
Max Magnitude | 1.2 |
rs4496877 is a SNP near the NOS3 gene.
Several Type-1 diabetes patients pools, totaling over 2,000 patients, plus a meta-analysis were involved in a study concluding that in such patients, the rs4496877 was associated with higher risk for nephropathy. The odds ratio associated with rs4496877(T) was 1.26 (p = 0.002, CI: 1.08-1.47).[PMID 20962522]
A proxy for this SNP (pairwise linkage of 0.96) is rs1800783.
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 19505917] Lead exposure, polymorphisms in genes related to oxidative stress, and risk of adult brain tumors.