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rs11684202

From SNPedia

Orientationplus
Stabilizedplus
Make rs11684202(A;A)
Make rs11684202(A;G)
Make rs11684202(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position25664689
GeneDTNB
is asnp
is mentioned by
dbSNPrs11684202
ebirs11684202
HLIrs11684202
Exacrs11684202
Varsomers11684202
Maprs11684202
PheGenIrs11684202
hapmaprs11684202
1000 genomesrs11684202
hgdprs11684202
ensemblrs11684202
gopubmedrs11684202
geneviewrs11684202
scholarrs11684202
googlers11684202
pharmgkbrs11684202
gwascentralrs11684202
openSNPrs11684202
23andMers11684202
23andMe allrs11684202
SNP Nexus

SNPshotrs11684202
SNPdbers11684202
MSV3drs11684202
GWAS Ctlgrs11684202
GMAF0.2475
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 0.000006
Odds Ratio 0.0938 [0.05-0.13] SD decrease