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rs1523288

From SNPedia

Orientationminus
Stabilizedminus
Make rs1523288(A;A)
Make rs1523288(A;G)
Make rs1523288(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position165562421
is asnp
is mentioned by
dbSNPrs1523288
ebirs1523288
HLIrs1523288
Exacrs1523288
Varsomers1523288
Maprs1523288
PheGenIrs1523288
hapmaprs1523288
1000 genomesrs1523288
hgdprs1523288
ensemblrs1523288
gopubmedrs1523288
geneviewrs1523288
scholarrs1523288
googlers1523288
pharmgkbrs1523288
gwascentralrs1523288
openSNPrs1523288
23andMers1523288
23andMe allrs1523288
SNP Nexus

SNPshotrs1523288
SNPdbers1523288
MSV3drs1523288
GWAS Ctlgrs1523288
GMAF0.3664
Max Magnitude
? (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 0.000006
Odds Ratio 1.15 [0.98-1.35]