Promethease 0.1.82
Rs10025771
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs10025771 |
| hapmap | rs10025771 |
| hgdp | rs10025771 |
| ensembl | rs10025771 |
| gopubmed | rs10025771 |
| scholar | rs10025771 |
| rs10025771 | |
| pharmgkb | rs10025771 |
| hgvbaseg2p | rs10025771 |
| medrefsnp | rs10025771 |
| 23andMe | rs10025771 |
| SNP Nexus |
| Gene | UGT2B17 |
| Orientation | plus |
| Position | 69087820 |
| Genotype | Effect |
|---|---|
| rs10025771(C;C)* | ? |
| rs10025771(C;T)* | ? |
| rs10025771(T;T)* | ? |
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."
