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rs1520832

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1520832(A;A)
Make rs1520832(A;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position42859612
is asnp
is mentioned by
dbSNPrs1520832
ebirs1520832
HLIrs1520832
Exacrs1520832
Varsomers1520832
Maprs1520832
PheGenIrs1520832
hapmaprs1520832
1000 genomesrs1520832
hgdprs1520832
ensemblrs1520832
gopubmedrs1520832
geneviewrs1520832
scholarrs1520832
googlers1520832
pharmgkbrs1520832
gwascentralrs1520832
openSNPrs1520832
23andMers1520832
23andMe allrs1520832
SNP Nexus

SNPshotrs1520832
SNPdbers1520832
MSV3drs1520832
GWAS Ctlgrs1520832
GMAF0.05464
Max Magnitude0
? (A;A) (A;C) (C;C) 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 0.000001
Odds Ratio 1.39 [0.99-1.95]