rs7913948
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7913948(A;A) |
Make rs7913948(A;G) |
Make rs7913948(G;G) |
Reference | GRCh37 37.1/131 |
Chromosome | 10 |
Position | 45373441 |
Gene | ALOX5 |
is a | snp |
is | mentioned by |
dbSNP | rs7913948 |
dbSNP (classic) | rs7913948 |
ClinGen | rs7913948 |
ebi | rs7913948 |
HLI | rs7913948 |
Exac | rs7913948 |
Gnomad | rs7913948 |
Varsome | rs7913948 |
LitVar | rs7913948 |
Map | rs7913948 |
PheGenI | rs7913948 |
Biobank | rs7913948 |
1000 genomes | rs7913948 |
hgdp | rs7913948 |
ensembl | rs7913948 |
geneview | rs7913948 |
scholar | rs7913948 |
rs7913948 | |
pharmgkb | rs7913948 |
gwascentral | rs7913948 |
openSNP | rs7913948 |
23andMe | rs7913948 |
SNPshot | rs7913948 |
SNPdbe | rs7913948 |
MSV3d | rs7913948 |
GWAS Ctlg | rs7913948 |
GMAF | 0.1777 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19787205] Association of genetic variants with myocardial infarction in individuals with or without hypertension or diabetes mellitus