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rs11669133

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs11669133(A;A)
Make rs11669133(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position10981463
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs11669133
ebirs11669133
HLIrs11669133
Exacrs11669133
Varsomers11669133
Maprs11669133
PheGenIrs11669133
hapmaprs11669133
1000 genomesrs11669133
hgdprs11669133
ensemblrs11669133
gopubmedrs11669133
geneviewrs11669133
scholarrs11669133
googlers11669133
pharmgkbrs11669133
gwascentralrs11669133
openSNPrs11669133
23andMers11669133
23andMe allrs11669133
SNP Nexus

SNPshotrs11669133
SNPdbers11669133
MSV3drs11669133
GWAS Ctlgrs11669133
GMAF0.03581
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 1E-8
Odds Ratio 0.1671 [0.11-0.23] SD decrease