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rs2824292

From SNPedia

Orientationplus
Stabilizedplus
Make rs2824292(A;A)
Make rs2824292(A;G)
Make rs2824292(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position17414857
is asnp
is mentioned by
dbSNPrs2824292
ebirs2824292
HLIrs2824292
Exacrs2824292
Varsomers2824292
Maprs2824292
PheGenIrs2824292
hapmaprs2824292
1000 genomesrs2824292
hgdprs2824292
ensemblrs2824292
gopubmedrs2824292
geneviewrs2824292
scholarrs2824292
googlers2824292
pharmgkbrs2824292
gwascentralrs2824292
openSNPrs2824292
23andMers2824292
23andMe allrs2824292
SNP Nexus

SNPshotrs2824292
SNPdbers2824292
MSV3drs2824292
GWAS Ctlgrs2824292
GMAF0.4559
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 24291282OA-icon.png] Coxsackie and adenovirus receptor (CAR) is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemia


[PMID 20622880OA-icon.png] Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction.


[PMID 21574885] No evidence for an association between the rs2824292 variant at chromosome 21q21 and ventricular fibrillation during acute myocardial infarction in a German population.