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rs548097

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs548097(A;C)
Make rs548097(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position75202132
is asnp
is mentioned by
dbSNPrs548097
ebirs548097
HLIrs548097
Exacrs548097
Varsomers548097
Maprs548097
PheGenIrs548097
hapmaprs548097
1000 genomesrs548097
hgdprs548097
ensemblrs548097
gopubmedrs548097
geneviewrs548097
scholarrs548097
googlers548097
pharmgkbrs548097
gwascentralrs548097
openSNPrs548097
23andMers548097
23andMe allrs548097
SNP Nexus

SNPshotrs548097
SNPdbers548097
MSV3drs548097
GWAS Ctlgrs548097
GMAF0.06198
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 6E-7
Odds Ratio 1.62 [1.00-2.63]