rs34547608
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs34547608(C;C) |
| Make rs34547608(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 233760182 |
| Gene | UGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34547608 |
| dbSNP (classic) | rs34547608 |
| ClinGen | rs34547608 |
| ebi | rs34547608 |
| HLI | rs34547608 |
| Exac | rs34547608 |
| Gnomad | rs34547608 |
| Varsome | rs34547608 |
| LitVar | rs34547608 |
| Map | rs34547608 |
| PheGenI | rs34547608 |
| Biobank | rs34547608 |
| 1000 genomes | rs34547608 |
| hgdp | rs34547608 |
| ensembl | rs34547608 |
| geneview | rs34547608 |
| scholar | rs34547608 |
| rs34547608 | |
| pharmgkb | rs34547608 |
| gwascentral | rs34547608 |
| openSNP | rs34547608 |
| 23andMe | rs34547608 |
| SNPshot | rs34547608 |
| SNPdbe | rs34547608 |
| MSV3d | rs34547608 |
| GWAS Ctlg | rs34547608 |
| GMAF | 0.02112 |
| Max Magnitude | 0 |
[PMID 21309756] Prevalence of clinically relevant UGT1A alleles and haplotypes in African populations
