rs6717546
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6717546(A;A) |
| Make rs6717546(A;G) |
| Make rs6717546(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 233773473 |
| Gene | MROH2A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6717546 |
| dbSNP (classic) | rs6717546 |
| ClinGen | rs6717546 |
| ebi | rs6717546 |
| HLI | rs6717546 |
| Exac | rs6717546 |
| Gnomad | rs6717546 |
| Varsome | rs6717546 |
| LitVar | rs6717546 |
| Map | rs6717546 |
| PheGenI | rs6717546 |
| Biobank | rs6717546 |
| 1000 genomes | rs6717546 |
| hgdp | rs6717546 |
| ensembl | rs6717546 |
| geneview | rs6717546 |
| scholar | rs6717546 |
| rs6717546 | |
| pharmgkb | rs6717546 |
| gwascentral | rs6717546 |
| openSNP | rs6717546 |
| 23andMe | rs6717546 |
| SNPshot | rs6717546 |
| SNPdbe | rs6717546 |
| MSV3d | rs6717546 |
| GWAS Ctlg | rs6717546 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24822274
] The effect of UGT1A and UGT2B polymorphisms on colorectal cancer risk: haplotype associations and gene–environment interactions
