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

rs11172782

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs11172782(A;G)
Make rs11172782(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position58865846
is asnp
is mentioned by
dbSNPrs11172782
ebirs11172782
HLIrs11172782
Exacrs11172782
Varsomers11172782
Maprs11172782
PheGenIrs11172782
hapmaprs11172782
1000 genomesrs11172782
hgdprs11172782
ensemblrs11172782
gopubmedrs11172782
geneviewrs11172782
scholarrs11172782
googlers11172782
pharmgkbrs11172782
gwascentralrs11172782
openSNPrs11172782
23andMers11172782
23andMe allrs11172782
SNP Nexus

SNPshotrs11172782
SNPdbers11172782
MSV3drs11172782
GWAS Ctlgrs11172782
GMAF0.1244
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20445134OA-icon.png]
Trait Heart failure
Title The Association of Genome-Wide Variation with the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis from the CHARGE Consortium
Risk Allele
P-val 7E-8
Odds Ratio 1.46 [1.03-2.09]