rs2540477
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2540477(C;C) |
Make rs2540477(C;T) |
Make rs2540477(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 96043776 |
Gene | LTA4H |
is a | snp |
is | mentioned by |
dbSNP | rs2540477 |
dbSNP (classic) | rs2540477 |
ClinGen | rs2540477 |
ebi | rs2540477 |
HLI | rs2540477 |
Exac | rs2540477 |
Gnomad | rs2540477 |
Varsome | rs2540477 |
LitVar | rs2540477 |
Map | rs2540477 |
PheGenI | rs2540477 |
Biobank | rs2540477 |
1000 genomes | rs2540477 |
hgdp | rs2540477 |
ensembl | rs2540477 |
geneview | rs2540477 |
scholar | rs2540477 |
rs2540477 | |
pharmgkb | rs2540477 |
gwascentral | rs2540477 |
openSNP | rs2540477 |
23andMe | rs2540477 |
SNPshot | rs2540477 |
SNPdbe | rs2540477 |
MSV3d | rs2540477 |
GWAS Ctlg | rs2540477 |
GMAF | 0.3384 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21293878] Genetic contribution of the leukotriene pathway to coronary artery disease
[PMID 30678701] Genetic variation in the leukotriene pathway is associated with myocardial infarction in the Chinese population.