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rs7323893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs7323893(C;C)
Make rs7323893(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position88052451
is asnp
is mentioned by
dbSNPrs7323893
ebirs7323893
HLIrs7323893
Exacrs7323893
Varsomers7323893
Maprs7323893
PheGenIrs7323893
hapmaprs7323893
1000 genomesrs7323893
hgdprs7323893
ensemblrs7323893
gopubmedrs7323893
geneviewrs7323893
scholarrs7323893
googlers7323893
pharmgkbrs7323893
gwascentralrs7323893
openSNPrs7323893
23andMers7323893
23andMe allrs7323893
SNP Nexus

SNPshotrs7323893
SNPdbers7323893
MSV3drs7323893
GWAS Ctlgrs7323893
GMAF0.02433
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 0.1360 [0.09-0.19] SD decrease