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rs13424957

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs13424957(C;T)
Make rs13424957(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position164893880
GeneLOC101929633
is asnp
is mentioned by
dbSNPrs13424957
ebirs13424957
HLIrs13424957
Exacrs13424957
Varsomers13424957
Maprs13424957
PheGenIrs13424957
hapmaprs13424957
1000 genomesrs13424957
hgdprs13424957
ensemblrs13424957
gopubmedrs13424957
geneviewrs13424957
scholarrs13424957
googlers13424957
pharmgkbrs13424957
gwascentralrs13424957
openSNPrs13424957
23andMers13424957
23andMe allrs13424957
SNP Nexus

SNPshotrs13424957
SNPdbers13424957
MSV3drs13424957
GWAS Ctlgrs13424957
GMAF0.05693
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
P-val 0.000003
Odds Ratio 1.2400 [1.14-1.36]