rs10025771
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10025771(C;C) |
| Make rs10025771(C;T) |
| Make rs10025771(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 68539507 |
| Gene | UGT2B17 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10025771 |
| dbSNP (classic) | rs10025771 |
| ClinGen | rs10025771 |
| ebi | rs10025771 |
| HLI | rs10025771 |
| Exac | rs10025771 |
| Gnomad | rs10025771 |
| Varsome | rs10025771 |
| LitVar | rs10025771 |
| Map | rs10025771 |
| PheGenI | rs10025771 |
| Biobank | rs10025771 |
| 1000 genomes | rs10025771 |
| hgdp | rs10025771 |
| ensembl | rs10025771 |
| geneview | rs10025771 |
| scholar | rs10025771 |
| rs10025771 | |
| pharmgkb | rs10025771 |
| gwascentral | rs10025771 |
| openSNP | rs10025771 |
| 23andMe | rs10025771 |
| SNPshot | rs10025771 |
| SNPdbe | rs10025771 |
| MSV3d | rs10025771 |
| GWAS Ctlg | rs10025771 |
| GMAF | 0.4986 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18334593] Deletion of both copies of this gene alters testosterone metabolism making steroid use undetectable.
The first page of this thesis claims that the deletion allele has a frequency of 4.8% in Swedes but is completely absent in Koreans. While its abstract claims "it is a common polymorphism with an allele frequency of 29 % in Swedes and 78 % in Koreans."
