rs7436338
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs7436338(A;A) |
| Make rs7436338(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 68567561 |
| Gene | UGT2B17 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7436338 |
| dbSNP (classic) | rs7436338 |
| ClinGen | rs7436338 |
| ebi | rs7436338 |
| HLI | rs7436338 |
| Exac | rs7436338 |
| Gnomad | rs7436338 |
| Varsome | rs7436338 |
| LitVar | rs7436338 |
| Map | rs7436338 |
| PheGenI | rs7436338 |
| Biobank | rs7436338 |
| 1000 genomes | rs7436338 |
| hgdp | rs7436338 |
| ensembl | rs7436338 |
| geneview | rs7436338 |
| scholar | rs7436338 |
| rs7436338 | |
| pharmgkb | rs7436338 |
| gwascentral | rs7436338 |
| openSNP | rs7436338 |
| 23andMe | rs7436338 |
| SNPshot | rs7436338 |
| SNPdbe | rs7436338 |
| MSV3d | rs7436338 |
| GWAS Ctlg | rs7436338 |
| GMAF | 0.02571 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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."
