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rs9546711

From SNPedia

Orientationplus
Stabilizedplus
Make rs9546711(A;A)
Make rs9546711(A;G)
Make rs9546711(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position84480131
GeneLINC00333
is asnp
is mentioned by
dbSNPrs9546711
ebirs9546711
HLIrs9546711
Exacrs9546711
Varsomers9546711
Maprs9546711
PheGenIrs9546711
hapmaprs9546711
1000 genomesrs9546711
hgdprs9546711
ensemblrs9546711
gopubmedrs9546711
geneviewrs9546711
scholarrs9546711
googlers9546711
pharmgkbrs9546711
gwascentralrs9546711
openSNPrs9546711
23andMers9546711
23andMe allrs9546711
SNP Nexus

SNPshotrs9546711
SNPdbers9546711
MSV3drs9546711
GWAS Ctlgrs9546711
GMAF0.225
Max Magnitude
? (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 0.000002
Odds Ratio 1.6600 [1.35-2.04]