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rs8017423

From SNPedia

Orientationplus
Stabilizedplus
Make rs8017423(C;C)
Make rs8017423(C;T)
Make rs8017423(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position90213566
is asnp
is mentioned by
dbSNPrs8017423
ebirs8017423
HLIrs8017423
Exacrs8017423
Varsomers8017423
Maprs8017423
PheGenIrs8017423
hapmaprs8017423
1000 genomesrs8017423
hgdprs8017423
ensemblrs8017423
gopubmedrs8017423
geneviewrs8017423
scholarrs8017423
googlers8017423
pharmgkbrs8017423
gwascentralrs8017423
openSNPrs8017423
23andMers8017423
23andMe allrs8017423
SNP Nexus

SNPshotrs8017423
SNPdbers8017423
MSV3drs8017423
GWAS Ctlgrs8017423
GMAF0.5
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20400778OA-icon.png]
Trait Mortality among heart failure patients
Title Genomic Variation Associated with Mortality among Adults of European and African Ancestry with Heart Failure: The CHARGE Consortium
Risk Allele T
P-val 0.000007
Odds Ratio 1.64 [0.94-2.78]