Have questions? Visit https://www.reddit.com/r/SNPedia

rs4876662

From SNPedia

Orientationplus
Stabilizedplus
Make rs4876662(A;A)
Make rs4876662(A;G)
Make rs4876662(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position116544032
is asnp
is mentioned by
dbSNPrs4876662
ebirs4876662
HLIrs4876662
Exacrs4876662
Varsomers4876662
Maprs4876662
PheGenIrs4876662
hapmaprs4876662
1000 genomesrs4876662
hgdprs4876662
ensemblrs4876662
gopubmedrs4876662
geneviewrs4876662
scholarrs4876662
googlers4876662
pharmgkbrs4876662
gwascentralrs4876662
openSNPrs4876662
23andMers4876662
23andMe allrs4876662
SNP Nexus

SNPshotrs4876662
SNPdbers4876662
MSV3drs4876662
GWAS Ctlgrs4876662
GMAF0.3039
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21223598OA-icon.png]
Trait
Title Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study
Risk Allele
P-val 0.000002
Odds Ratio 0.1317 [0.081-0.182] cm increase