rs11185660
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11185660(C;C) |
| Make rs11185660(C;T) |
| Make rs11185660(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 134368146 |
| Gene | RXRA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11185660 |
| dbSNP (classic) | rs11185660 |
| ClinGen | rs11185660 |
| ebi | rs11185660 |
| HLI | rs11185660 |
| Exac | rs11185660 |
| Gnomad | rs11185660 |
| Varsome | rs11185660 |
| LitVar | rs11185660 |
| Map | rs11185660 |
| PheGenI | rs11185660 |
| Biobank | rs11185660 |
| 1000 genomes | rs11185660 |
| hgdp | rs11185660 |
| ensembl | rs11185660 |
| geneview | rs11185660 |
| scholar | rs11185660 |
| rs11185660 | |
| pharmgkb | rs11185660 |
| gwascentral | rs11185660 |
| openSNP | rs11185660 |
| 23andMe | rs11185660 |
| SNPshot | rs11185660 |
| SNPdbe | rs11185660 |
| MSV3d | rs11185660 |
| GWAS Ctlg | rs11185660 |
| GMAF | 0.2975 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20855565
] Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease
