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rs503662

From SNPedia

Orientationminus
Stabilizedminus
Make rs503662(A;A)
Make rs503662(A;G)
Make rs503662(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position21191270
is asnp
is mentioned by
dbSNPrs503662
ebirs503662
HLIrs503662
Exacrs503662
Varsomers503662
Maprs503662
PheGenIrs503662
hapmaprs503662
1000 genomesrs503662
hgdprs503662
ensemblrs503662
gopubmedrs503662
geneviewrs503662
scholarrs503662
googlers503662
pharmgkbrs503662
gwascentralrs503662
openSNPrs503662
23andMers503662
23andMe allrs503662
SNP Nexus

SNPshotrs503662
SNPdbers503662
MSV3drs503662
GWAS Ctlgrs503662
GMAF0.303
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 23653095OA-icon.png] Positive correlation between variants of lipid metabolism‑related genes and coronary heart disease


[PMID 21347282OA-icon.png] Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.