rs5839491
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | normal risk | |
| (-;AT) | some effects of higher bilirubin | |
| (AT;AT) | effects of higher bilirubin; irinotecan toxicity |
| Reference | GRCh37.p2 37.2/134 |
| Chromosome | 2 |
| Position | 234668885 |
| Gene | UGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5839491 |
| dbSNP (classic) | rs5839491 |
| ClinGen | rs5839491 |
| ebi | rs5839491 |
| HLI | rs5839491 |
| Exac | rs5839491 |
| Gnomad | rs5839491 |
| Varsome | rs5839491 |
| LitVar | rs5839491 |
| Map | rs5839491 |
| PheGenI | rs5839491 |
| Biobank | rs5839491 |
| 1000 genomes | rs5839491 |
| hgdp | rs5839491 |
| ensembl | rs5839491 |
| geneview | rs5839491 |
| scholar | rs5839491 |
| rs5839491 | |
| pharmgkb | rs5839491 |
| gwascentral | rs5839491 |
| openSNP | rs5839491 |
| 23andMe | rs5839491 |
| SNPshot | rs5839491 |
| SNPdbe | rs5839491 |
| MSV3d | rs5839491 |
| GWAS Ctlg | rs5839491 |
| Status | Deleted |
| Max Magnitude | 0 |
rs5839491 is one of four SNPs all describing an insertion/deletion polymorphism in the promoter region of the UGT1A1 gene; the primary entry in SNPedia for this set of SNPs is at rs34815109.
The other two SNPs (besides rs34815109) that also describe the same polymorphism are:
[PMID 20528568] Evaluation of UGT1A1 and SULT1A1 polymorphisms with lipid levels in women with different hormonal status.
