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rs2046383

From SNPedia

Orientationplus
Stabilizedplus
Make rs2046383(G;G)
Make rs2046383(G;T)
Make rs2046383(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position29951209
is asnp
is mentioned by
dbSNPrs2046383
ebirs2046383
HLIrs2046383
Exacrs2046383
Varsomers2046383
Maprs2046383
PheGenIrs2046383
hapmaprs2046383
1000 genomesrs2046383
hgdprs2046383
ensemblrs2046383
gopubmedrs2046383
geneviewrs2046383
scholarrs2046383
googlers2046383
pharmgkbrs2046383
gwascentralrs2046383
openSNPrs2046383
23andMers2046383
23andMe allrs2046383
SNP Nexus

SNPshotrs2046383
SNPdbers2046383
MSV3drs2046383
GWAS Ctlgrs2046383
GMAF0.2948
Max Magnitude
? (G;G) (G;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 0.000003
Odds Ratio 1.39 [0.97-1.97]