rs7861779
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 2 |
| Make rs7861779(C;C) |
| Make rs7861779(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 134417615 |
| Gene | RXRA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7861779 |
| dbSNP (classic) | rs7861779 |
| ClinGen | rs7861779 |
| ebi | rs7861779 |
| HLI | rs7861779 |
| Exac | rs7861779 |
| Gnomad | rs7861779 |
| Varsome | rs7861779 |
| LitVar | rs7861779 |
| Map | rs7861779 |
| PheGenI | rs7861779 |
| Biobank | rs7861779 |
| 1000 genomes | rs7861779 |
| hgdp | rs7861779 |
| ensembl | rs7861779 |
| geneview | rs7861779 |
| scholar | rs7861779 |
| rs7861779 | |
| pharmgkb | rs7861779 |
| gwascentral | rs7861779 |
| openSNP | rs7861779 |
| 23andMe | rs7861779 |
| SNPshot | rs7861779 |
| SNPdbe | rs7861779 |
| MSV3d | rs7861779 |
| GWAS Ctlg | rs7861779 |
| GMAF | 0.2309 |
| Max Magnitude | 2 |
[PMID 20145122
] Genetic Polymorphisms in Vitamin D Receptor VDR/RXRA Influence the Likelihood of Colon Adenoma Recurrence
[PMID 20558521] Genetic variation in the retinoid X receptor and calcium-sensing receptor, and risk of colorectal cancer in the Colon Cancer Family Registry
