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rs4979906

From SNPedia

Orientationplus
Stabilizedplus
Make rs4979906(A;A)
Make rs4979906(A;G)
Make rs4979906(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position77684995
is asnp
is mentioned by
dbSNPrs4979906
ebirs4979906
HLIrs4979906
Exacrs4979906
Varsomers4979906
Maprs4979906
PheGenIrs4979906
hapmaprs4979906
1000 genomesrs4979906
hgdprs4979906
ensemblrs4979906
gopubmedrs4979906
geneviewrs4979906
scholarrs4979906
googlers4979906
pharmgkbrs4979906
gwascentralrs4979906
openSNPrs4979906
23andMers4979906
23andMe allrs4979906
SNP Nexus

SNPshotrs4979906
SNPdbers4979906
MSV3drs4979906
GWAS Ctlgrs4979906
GMAF0.3494
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 0.000007
Odds Ratio 1.23 [0.98-1.55]