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rs7569328

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7569328(C;T)
Make rs7569328(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position20901018
is asnp
is mentioned by
dbSNPrs7569328
ebirs7569328
HLIrs7569328
Exacrs7569328
Varsomers7569328
Maprs7569328
PheGenIrs7569328
hapmaprs7569328
1000 genomesrs7569328
hgdprs7569328
ensemblrs7569328
gopubmedrs7569328
geneviewrs7569328
scholarrs7569328
googlers7569328
pharmgkbrs7569328
gwascentralrs7569328
openSNPrs7569328
23andMers7569328
23andMe allrs7569328
SNP Nexus

SNPshotrs7569328
SNPdbers7569328
MSV3drs7569328
GWAS Ctlgrs7569328
GMAF0.04959
Max Magnitude0
? (C;C) (C;T) (T;T) 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 T
P-val 1E-7
Odds Ratio 0.0995 [0.06-0.14] SD decrease