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rs12269901

From SNPedia

Orientationplus
Stabilizedplus
Make rs12269901(C;C)
Make rs12269901(C;G)
Make rs12269901(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position117103213
is asnp
is mentioned by
dbSNPrs12269901
ebirs12269901
HLIrs12269901
Exacrs12269901
Varsomers12269901
Maprs12269901
PheGenIrs12269901
hapmaprs12269901
1000 genomesrs12269901
hgdprs12269901
ensemblrs12269901
gopubmedrs12269901
geneviewrs12269901
scholarrs12269901
googlers12269901
pharmgkbrs12269901
gwascentralrs12269901
openSNPrs12269901
23andMers12269901
23andMe allrs12269901
SNP Nexus

SNPshotrs12269901
SNPdbers12269901
MSV3drs12269901
GWAS Ctlgrs12269901
GMAF0.3949
Max Magnitude
? (C;C) (C;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 C
P-val 0.000002
Odds Ratio 0.0690 [0.04-0.10] SD increase