rs11902417
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11902417(A;A) |
Make rs11902417(A;G) |
Make rs11902417(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 20976028 |
is a | snp |
is | mentioned by |
dbSNP | rs11902417 |
dbSNP (classic) | rs11902417 |
ClinGen | rs11902417 |
ebi | rs11902417 |
HLI | rs11902417 |
Exac | rs11902417 |
Gnomad | rs11902417 |
Varsome | rs11902417 |
LitVar | rs11902417 |
Map | rs11902417 |
PheGenI | rs11902417 |
Biobank | rs11902417 |
1000 genomes | rs11902417 |
hgdp | rs11902417 |
ensembl | rs11902417 |
geneview | rs11902417 |
scholar | rs11902417 |
rs11902417 | |
pharmgkb | rs11902417 |
gwascentral | rs11902417 |
openSNP | rs11902417 |
23andMe | rs11902417 |
SNPshot | rs11902417 |
SNPdbe | rs11902417 |
MSV3d | rs11902417 |
GWAS Ctlg | rs11902417 |
GMAF | 0.3535 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20864672] |
Trait | |
Title | Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease |
Risk Allele | G |
P-val | 4E-7 |
Odds Ratio | 0.02 [0.01-0.03] unit decrease |