rs3818569
From SNPedia
| Merged into | rs1128977 |
| Orientation | minus |
| Stabilized | minus |
| Make rs3818569(C;C) |
| Make rs3818569(C;T) |
| Make rs3818569(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 165419892 |
| Gene | RXRG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3818569 |
| dbSNP (classic) | rs3818569 |
| ClinGen | rs3818569 |
| ebi | rs3818569 |
| HLI | rs3818569 |
| Exac | rs3818569 |
| Gnomad | rs3818569 |
| Varsome | rs3818569 |
| LitVar | rs3818569 |
| Map | rs3818569 |
| PheGenI | rs3818569 |
| Biobank | rs3818569 |
| 1000 genomes | rs3818569 |
| hgdp | rs3818569 |
| ensembl | rs3818569 |
| geneview | rs3818569 |
| scholar | rs3818569 |
| rs3818569 | |
| pharmgkb | rs3818569 |
| gwascentral | rs3818569 |
| openSNP | rs3818569 |
| 23andMe | rs3818569 |
| SNPshot | rs3818569 |
| SNPdbe | rs3818569 |
| MSV3d | rs3818569 |
| GWAS Ctlg | rs3818569 |
| Status | Merged into rs1128977 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22180072] Association between retinoid-X receptor-gamma genetic polymorphisms and diabetic retinopathy
[PMID 25867398] Associations between genetic variants and the severity of metabolic syndrome in subjects with type 2 diabetes
