rs3882891
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3882891(A;A) |
Make rs3882891(A;C) |
Make rs3882891(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 112144038 |
Gene | IL18 |
is a | snp |
is | mentioned by |
dbSNP | rs3882891 |
dbSNP (classic) | rs3882891 |
ClinGen | rs3882891 |
ebi | rs3882891 |
HLI | rs3882891 |
Exac | rs3882891 |
Gnomad | rs3882891 |
Varsome | rs3882891 |
LitVar | rs3882891 |
Map | rs3882891 |
PheGenI | rs3882891 |
Biobank | rs3882891 |
1000 genomes | rs3882891 |
hgdp | rs3882891 |
ensembl | rs3882891 |
geneview | rs3882891 |
scholar | rs3882891 |
rs3882891 | |
pharmgkb | rs3882891 |
gwascentral | rs3882891 |
openSNP | rs3882891 |
23andMe | rs3882891 |
SNPshot | rs3882891 |
SNPdbe | rs3882891 |
MSV3d | rs3882891 |
GWAS Ctlg | rs3882891 |
GMAF | 0.4982 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 22015107] Interleukin 18 gene variation and risk of acute myocardial infarction
[PMID 20227263] Genetic variation within IL18 is associated with insulin levels, insulin resistance and postprandial measures.