Have questions? Visit https://www.reddit.com/r/SNPedia

rs5744241

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs5744241(A;G)
Make rs5744241(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position112156421
GeneIL18
is asnp
is mentioned by
dbSNPrs5744241
ebirs5744241
HLIrs5744241
Exacrs5744241
Varsomers5744241
Maprs5744241
PheGenIrs5744241
hapmaprs5744241
1000 genomesrs5744241
hgdprs5744241
ensemblrs5744241
gopubmedrs5744241
geneviewrs5744241
scholarrs5744241
googlers5744241
pharmgkbrs5744241
gwascentralrs5744241
openSNPrs5744241
23andMers5744241
23andMe allrs5744241
SNP Nexus

SNPshotrs5744241
SNPdbers5744241
MSV3drs5744241
GWAS Ctlgrs5744241
GMAF0.03994
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 22015107] Interleukin 18 gene variation and risk of acute myocardial infarction


[PMID 20478055OA-icon.png] Evaluation of 6 candidate genes on chromosome 11q23 for coeliac disease susceptibility: a case control study.