rs10889160
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs10889160(A;A) |
Make rs10889160(A;G) |
Make rs10889160(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 59896449 |
Gene | CYP2J2 |
is a | snp |
is | mentioned by |
dbSNP | rs10889160 |
dbSNP (classic) | rs10889160 |
ClinGen | rs10889160 |
ebi | rs10889160 |
HLI | rs10889160 |
Exac | rs10889160 |
Gnomad | rs10889160 |
Varsome | rs10889160 |
LitVar | rs10889160 |
Map | rs10889160 |
PheGenI | rs10889160 |
Biobank | rs10889160 |
1000 genomes | rs10889160 |
hgdp | rs10889160 |
ensembl | rs10889160 |
geneview | rs10889160 |
scholar | rs10889160 |
rs10889160 | |
pharmgkb | rs10889160 |
gwascentral | rs10889160 |
openSNP | rs10889160 |
23andMe | rs10889160 |
SNPshot | rs10889160 |
SNPdbe | rs10889160 |
MSV3d | rs10889160 |
GWAS Ctlg | rs10889160 |
GMAF | 0.2351 |
Max Magnitude | 0 |
A study of 858 cases concluded that SNPs in the intron of the CYP2J2 gene were associated with increased risk for myocardial infarction. rs10889160 had an odds ratio of 1.24, CI: 1.07-1.43, p=0.004.[PMID 18496133]