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rs13225783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs13225783(C;T)
Make rs13225783(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position27290437
is asnp
is mentioned by
dbSNPrs13225783
ebirs13225783
HLIrs13225783
Exacrs13225783
Varsomers13225783
Maprs13225783
PheGenIrs13225783
hapmaprs13225783
1000 genomesrs13225783
hgdprs13225783
ensemblrs13225783
gopubmedrs13225783
geneviewrs13225783
scholarrs13225783
googlers13225783
pharmgkbrs13225783
gwascentralrs13225783
openSNPrs13225783
23andMers13225783
23andMe allrs13225783
SNP Nexus

SNPshotrs13225783
SNPdbers13225783
MSV3drs13225783
GWAS Ctlgrs13225783
GMAF0.02112
Max Magnitude0
? (C;C) (C;T) (T;T) 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 0.000007
Odds Ratio 1.38 [0.96-1.99]