rs5001812
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs5001812(G;G) |
Make rs5001812(G;T) |
Make rs5001812(T;T) |
Reference | GRCh37.p5 37.3/137 |
Chromosome | 2 |
Position | 166704294 |
is a | snp |
is | mentioned by |
dbSNP | rs5001812 |
dbSNP (classic) | rs5001812 |
ClinGen | rs5001812 |
ebi | rs5001812 |
HLI | rs5001812 |
Exac | rs5001812 |
Gnomad | rs5001812 |
Varsome | rs5001812 |
LitVar | rs5001812 |
Map | rs5001812 |
PheGenI | rs5001812 |
Biobank | rs5001812 |
1000 genomes | rs5001812 |
hgdp | rs5001812 |
ensembl | rs5001812 |
geneview | rs5001812 |
scholar | rs5001812 |
rs5001812 | |
pharmgkb | rs5001812 |
gwascentral | rs5001812 |
openSNP | rs5001812 |
23andMe | rs5001812 |
SNPshot | rs5001812 |
SNPdbe | rs5001812 |
MSV3d | rs5001812 |
GWAS Ctlg | rs5001812 |
Status | Deleted |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22890011] |
Trait | Response to fenofibrate |
Title | Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate. |
Risk Allele | T |
P-val | 2E-7 |
Odds Ratio | 4.67 [2.93-6.41] unit decrease |