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rs11880198

From SNPedia

Orientationplus
Stabilizedplus
Make rs11880198(A;A)
Make rs11880198(A;G)
Make rs11880198(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position3159771
GeneGNA15
is asnp
is mentioned by
dbSNPrs11880198
ebirs11880198
HLIrs11880198
Exacrs11880198
Varsomers11880198
Maprs11880198
PheGenIrs11880198
hapmaprs11880198
1000 genomesrs11880198
hgdprs11880198
ensemblrs11880198
gopubmedrs11880198
geneviewrs11880198
scholarrs11880198
googlers11880198
pharmgkbrs11880198
gwascentralrs11880198
openSNPrs11880198
23andMers11880198
23andMe allrs11880198
SNP Nexus

SNPshotrs11880198
SNPdbers11880198
MSV3drs11880198
GWAS Ctlgrs11880198
GMAF0.1433
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 1.23 [0.98-1.54]