Have questions? Visit https://www.reddit.com/r/SNPedia

rs3729639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs3729639(C;T)
Make rs3729639(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position67191598
GeneEXOC3L, E2F4
is asnp
is mentioned by
dbSNPrs3729639
ebirs3729639
HLIrs3729639
Exacrs3729639
Varsomers3729639
Maprs3729639
PheGenIrs3729639
hapmaprs3729639
1000 genomesrs3729639
hgdprs3729639
ensemblrs3729639
gopubmedrs3729639
geneviewrs3729639
scholarrs3729639
googlers3729639
pharmgkbrs3729639
gwascentralrs3729639
openSNPrs3729639
23andMers3729639
23andMe allrs3729639
SNP Nexus

SNPshotrs3729639
SNPdbers3729639
MSV3drs3729639
GWAS Ctlgrs3729639
GMAF0.152
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 2E-11
Odds Ratio 0.0900 [0.06-0.12] SD increase