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rs5904726

From SNPedia

Orientationplus
Stabilizedplus
Make rs5904726(A;A)
Make rs5904726(A;G)
Make rs5904726(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position147241105
is asnp
is mentioned by
dbSNPrs5904726
ebirs5904726
HLIrs5904726
Exacrs5904726
Varsomers5904726
Maprs5904726
PheGenIrs5904726
hapmaprs5904726
1000 genomesrs5904726
hgdprs5904726
ensemblrs5904726
gopubmedrs5904726
geneviewrs5904726
scholarrs5904726
googlers5904726
pharmgkbrs5904726
gwascentralrs5904726
openSNPrs5904726
23andMers5904726
23andMe allrs5904726
SNP Nexus

SNPshotrs5904726
SNPdbers5904726
MSV3drs5904726
GWAS Ctlgrs5904726
GMAF0.3646
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21347282OA-icon.png]
Trait
Title Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
Risk Allele A
P-val 0.000009
Odds Ratio 0.0639 [0.03-0.09] SD increase