rs186021206
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs186021206(A;A) |
| Make rs186021206(A;G) |
| Make rs186021206(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 17 |
| Position | 7166093 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs186021206 |
| dbSNP (classic) | rs186021206 |
| ClinGen | rs186021206 |
| ebi | rs186021206 |
| HLI | rs186021206 |
| Exac | rs186021206 |
| Gnomad | rs186021206 |
| Varsome | rs186021206 |
| LitVar | rs186021206 |
| Map | rs186021206 |
| PheGenI | rs186021206 |
| Biobank | rs186021206 |
| 1000 genomes | rs186021206 |
| hgdp | rs186021206 |
| ensembl | rs186021206 |
| geneview | rs186021206 |
| scholar | rs186021206 |
| rs186021206 | |
| pharmgkb | rs186021206 |
| gwascentral | rs186021206 |
| openSNP | rs186021206 |
| 23andMe | rs186021206 |
| SNPshot | rs186021206 |
| SNPdbe | rs186021206 |
| MSV3d | rs186021206 |
| GWAS Ctlg | rs186021206 |
| Max Magnitude | 0 |
This SNP is a proxy for the in/del variants discussed on the ASGR1 page; these variants are associated with lowered risk for myocardial infarction and coronary artery disease.
