rs11726269
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11726269(A;A) |
Make rs11726269(A;G) |
Make rs11726269(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 86311831 |
Gene | MAPK10 |
is a | snp |
is | mentioned by |
dbSNP | rs11726269 |
dbSNP (classic) | rs11726269 |
ClinGen | rs11726269 |
ebi | rs11726269 |
HLI | rs11726269 |
Exac | rs11726269 |
Gnomad | rs11726269 |
Varsome | rs11726269 |
LitVar | rs11726269 |
Map | rs11726269 |
PheGenI | rs11726269 |
Biobank | rs11726269 |
1000 genomes | rs11726269 |
hgdp | rs11726269 |
ensembl | rs11726269 |
geneview | rs11726269 |
scholar | rs11726269 |
rs11726269 | |
pharmgkb | rs11726269 |
gwascentral | rs11726269 |
openSNP | rs11726269 |
23andMe | rs11726269 |
SNPshot | rs11726269 |
SNPdbe | rs11726269 |
MSV3d | rs11726269 |
GWAS Ctlg | rs11726269 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 25009551] |
Trait | Peripheral artery disease |
Title | The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study. |
Risk Allele | G |
P-val | 2E-6 |
Odds Ratio | 1.39 [1.22-1.59] |