rs7662029
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7662029(A;A) |
| Make rs7662029(A;G) |
| Make rs7662029(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 4 |
| Position | 69096194 |
| Gene | UGT2B7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7662029 |
| dbSNP (classic) | rs7662029 |
| ClinGen | rs7662029 |
| ebi | rs7662029 |
| HLI | rs7662029 |
| Exac | rs7662029 |
| Gnomad | rs7662029 |
| Varsome | rs7662029 |
| LitVar | rs7662029 |
| Map | rs7662029 |
| PheGenI | rs7662029 |
| Biobank | rs7662029 |
| 1000 genomes | rs7662029 |
| hgdp | rs7662029 |
| ensembl | rs7662029 |
| geneview | rs7662029 |
| scholar | rs7662029 |
| rs7662029 | |
| pharmgkb | rs7662029 |
| gwascentral | rs7662029 |
| openSNP | rs7662029 |
| 23andMe | rs7662029 |
| SNPshot | rs7662029 |
| SNPdbe | rs7662029 |
| MSV3d | rs7662029 |
| GWAS Ctlg | rs7662029 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 28524801] Association of UGT2B7, UGT1A9, ABCG2, and IL23R polymorphisms with rejection risk in kidney transplant patients.
