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rs6544366

From SNPedia

Orientationplus
Stabilizedplus
Make rs6544366(G;G)
Make rs6544366(G;T)
Make rs6544366(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position20981153
is asnp
is mentioned by
dbSNPrs6544366
ebirs6544366
HLIrs6544366
Exacrs6544366
Varsomers6544366
Maprs6544366
PheGenIrs6544366
hapmaprs6544366
1000 genomesrs6544366
hgdprs6544366
ensemblrs6544366
gopubmedrs6544366
geneviewrs6544366
scholarrs6544366
googlers6544366
pharmgkbrs6544366
gwascentralrs6544366
openSNPrs6544366
23andMers6544366
23andMe allrs6544366
SNP Nexus

SNPshotrs6544366
SNPdbers6544366
MSV3drs6544366
GWAS Ctlgrs6544366
GMAF0.3476
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20864672OA-icon.png]
Trait
Title Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Risk Allele T
P-val 2E-7
Odds Ratio 0.04 [0.03-0.05] unit decrease