rs11684202
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11684202(A;A) |
Make rs11684202(A;G) |
Make rs11684202(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 25664689 |
Gene | DTNB |
is a | snp |
is | mentioned by |
dbSNP | rs11684202 |
dbSNP (classic) | rs11684202 |
ClinGen | rs11684202 |
ebi | rs11684202 |
HLI | rs11684202 |
Exac | rs11684202 |
Gnomad | rs11684202 |
Varsome | rs11684202 |
LitVar | rs11684202 |
Map | rs11684202 |
PheGenI | rs11684202 |
Biobank | rs11684202 |
1000 genomes | rs11684202 |
hgdp | rs11684202 |
ensembl | rs11684202 |
geneview | rs11684202 |
scholar | rs11684202 |
rs11684202 | |
pharmgkb | rs11684202 |
gwascentral | rs11684202 |
openSNP | rs11684202 |
23andMe | rs11684202 |
SNPshot | rs11684202 |
SNPdbe | rs11684202 |
MSV3d | rs11684202 |
GWAS Ctlg | rs11684202 |
GMAF | 0.2475 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21347282] |
Trait | |
Title | Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project |
Risk Allele | A |
P-val | 0.000006 |
Odds Ratio | 0.0938 [0.05-0.13] SD decrease |