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rs12239436

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs12239436(A;A)
Make rs12239436(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position55277164
is asnp
is mentioned by
dbSNPrs12239436
ebirs12239436
HLIrs12239436
Exacrs12239436
Varsomers12239436
Maprs12239436
PheGenIrs12239436
hapmaprs12239436
1000 genomesrs12239436
hgdprs12239436
ensemblrs12239436
gopubmedrs12239436
geneviewrs12239436
scholarrs12239436
googlers12239436
pharmgkbrs12239436
gwascentralrs12239436
openSNPrs12239436
23andMers12239436
23andMe allrs12239436
SNP Nexus

SNPshotrs12239436
SNPdbers12239436
MSV3drs12239436
GWAS Ctlgrs12239436
GMAF0.02617
Max Magnitude0
? (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 0.000005
Odds Ratio 0.0928 [0.05-0.13] SD increase