UGT2B15
UDP glucuronosyltransferase family 2 member B15
Pharmacogene
Summary
This gene encodes a glycosyltransferase that is invovled in the metabolism and elimination of toxic compounts, both endogenous and of xenobiotic origin. This gene plays a role in the regulation of estrogens and androgens. This locus is present in a cluster of similar genes and pseudogenes on chromosome 4. [provided by RefSeq, Aug 2016]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs143480699 | 4:68,647,145 | G/A | stop gained | — |
| rs148583958 | 4:68,655,133 | G/A | missense variant | — |
| rs368012995 | 4:68,670,362 | A/G | missense variant | — |
| rs3100 | 4:69,512,654 | G/T | — | — |
| rs146711063 | 4:69,512,835 | T/C | — | benign |
| rs4148269 | 4:69,512,847 | T/C | missense variant | — |
| rs779082639 | 4:69,512,877 | C/T | — | uncertain significance |
| rs370288795 | 4:69,512,908 | C/T | — | uncertain significance |
| rs150032309 | 4:69,512,911 | C/T | — | uncertain significance |
| rs142432791 | 4:69,512,929 | C/T | — | uncertain significance |
| rs1182928744 | 4:69,512,956 | T/A | — | uncertain significance |
| rs147164238 | 4:69,513,007 | G/T | — | uncertain significance |
| rs1480411884 | 4:69,513,055 | G/A | — | uncertain significance |
| rs2476198361 | 4:69,513,084 | A/G | — | uncertain significance |
| rs6837575 | 4:69,514,963 | G/T | — | — |
| rs568044905 | 4:69,519,789 | G/A | — | uncertain significance |
| rs1333723789 | 4:69,519,815 | A/T | — | uncertain significance |
| rs1490310763 | 4:69,519,823 | A/T | — | likely benign |
| rs376250826 | 4:69,519,849 | T/C | — | uncertain significance |
| rs553126424 | 4:69,519,881 | A/G | — | uncertain significance |
| rs2476212002 | 4:69,519,885 | G/C | — | uncertain significance |
| rs1409040989 | 4:69,519,915 | T/C | — | uncertain significance |
| rs767150720 | 4:69,519,917 | G/A | — | uncertain significance |
| rs369450796 | 4:69,520,819 | G/A | — | uncertain significance |
| rs760572886 | 4:69,520,846 | G/C | — | uncertain significance |
| rs751655131 | 4:69,520,855 | T/G | — | uncertain significance |
| rs767776292 | 4:69,520,860 | C/A | — | uncertain significance |
| rs142948482 | 4:69,520,867 | T/A | — | conflicting classifications of pathogenicity |
| rs78520527 | 4:69,526,612 | A/C | — | — |
| rs768568429 | 4:69,528,748 | G/C | — | uncertain significance |
| rs1330953077 | 4:69,528,757 | A/G | — | uncertain significance |
| rs1235492872 | 4:69,528,835 | C/A | — | uncertain significance |
| rs1531022 | 4:69,532,128 | G/C | — | — |
| rs1349852 | 4:69,533,217 | A/C | — | — |
| rs989075 | 4:69,533,221 | A/C | — | — |
| rs2045100 | 4:69,533,702 | T/C | — | — |
| rs1993282 | 4:69,533,749 | T/C | — | benign |
| rs150398834 | 4:69,533,826 | G/A | — | uncertain significance |
| rs746006788 | 4:69,533,891 | A/G | — | uncertain significance |
| rs772287563 | 4:69,535,634 | G/C | — | uncertain significance |
| rs569291276 | 4:69,535,722 | T/G | — | uncertain significance |
| rs143136322 | 4:69,535,754 | C/T | — | uncertain significance |
| rs377015117 | 4:69,535,816 | C/T | — | uncertain significance |
| rs760993055 | 4:69,535,841 | T/G | — | uncertain significance |
| rs773298043 | 4:69,535,886 | C/T | — | uncertain significance |
| rs752755239 | 4:69,535,895 | C/G | — | uncertain significance |
| rs371266915 | 4:69,535,963 | T/C | — | uncertain significance |
| rs2476245774 | 4:69,536,018 | A/C | — | uncertain significance |
| rs1560613361 | 4:69,536,021 | A/G | — | uncertain significance |
| rs767748124 | 4:69,536,054 | C/A | — | uncertain significance |
| rs1902023 | 4:69,536,084 | A/C | missense | — |
| rs1733276432 | 4:69,536,140 | G/A | — | uncertain significance |
| rs74987674 | 4:69,536,163 | A/C | — | benign |
| rs2476246484 | 4:69,536,180 | C/T | — | uncertain significance |
| rs149630676 | 4:69,536,191 | C/T | — | uncertain significance |
| rs747026246 | 4:69,536,280 | G/T | — | uncertain significance |
| rs771229536 | 4:69,536,281 | C/T | — | uncertain significance |
| rs374449593 | 4:69,536,294 | T/C | — | uncertain significance |
| rs1580083 | 4:69,536,842 | A/T | — | — |
| rs1960773 | 4:69,537,154 | A/T | — | — |
| rs9994887 | 4:69,537,475 | A/G | upstream gene variant | — |
| rs13112099 | 4:69,537,733 | T/C | — | — |
| rs7686914 | 4:69,537,915 | T/C | upstream gene variant | — |
| rs7696472 | 4:69,538,180 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.