UGT2B10
UDP glucuronosyltransferase family 2 member B10
Summary
Predicted to enable UDP-glycosyltransferase activity. Predicted to be involved in estrogen metabolic process. Predicted to be located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs294775 | 4:69,680,933 | C/T | upstream gene variant | — |
| rs11725502 | 4:69,680,942 | A/T | upstream gene variant | — |
| rs1263567182 | 4:69,681,769 | T/C | — | uncertain significance |
| rs760152967 | 4:69,681,799 | G/A | — | uncertain significance |
| rs770357735 | 4:69,681,869 | A/C | — | uncertain significance |
| rs61750900 | 4:69,681,936 | G/T | missense variant | — |
| rs2529324775 | 4:69,682,054 | T/C | — | likely benign |
| rs895046142 | 4:69,682,074 | G/A | — | uncertain significance |
| rs749384384 | 4:69,682,084 | G/C | — | uncertain significance |
| rs755594714 | 4:69,682,116 | A/G | — | uncertain significance |
| rs748774493 | 4:69,682,125 | G/C | — | uncertain significance |
| rs747983652 | 4:69,682,137 | A/C | — | uncertain significance |
| rs760720595 | 4:69,682,143 | A/C | — | uncertain significance |
| rs770772934 | 4:69,682,144 | T/C | — | uncertain significance |
| rs2529325296 | 4:69,682,167 | T/C | — | uncertain significance |
| rs199569934 | 4:69,682,185 | G/C | — | uncertain significance |
| rs200419731 | 4:69,682,188 | G/T | — | uncertain significance |
| rs1479686148 | 4:69,682,238 | T/G | — | likely benign |
| rs754545207 | 4:69,682,249 | A/G | — | uncertain significance |
| rs762324444 | 4:69,682,317 | C/T | — | uncertain significance |
| rs562436137 | 4:69,682,320 | G/A | — | uncertain significance |
| rs2529326526 | 4:69,682,401 | T/C | — | uncertain significance |
| rs779971456 | 4:69,682,402 | G/C | — | uncertain significance |
| rs754926782 | 4:69,682,412 | A/G | — | uncertain significance |
| rs2529326693 | 4:69,682,441 | A/C | — | uncertain significance |
| rs294777 | 4:69,682,471 | A/G | regulatory region variant | — |
| rs294778 | 4:69,682,555 | G/T | — | — |
| rs7657958 | 4:69,682,795 | G/A | regulatory region variant | — |
| rs1215237960 | 4:69,683,759 | C/G | — | uncertain significance |
| rs201500332 | 4:69,683,801 | G/A | — | uncertain significance |
| rs368183985 | 4:69,683,831 | C/T | — | uncertain significance |
| rs2529331274 | 4:69,683,836 | T/G | — | uncertain significance |
| rs373059693 | 4:69,683,885 | C/T | — | uncertain significance |
| rs835315 | 4:69,685,772 | G/A | intron variant | — |
| rs2942857 | 4:69,687,987 | C/A | splice region variant | — |
| rs2670430 | 4:69,689,122 | C/G | intron variant | — |
| rs1440549240 | 4:69,692,141 | T/A | — | uncertain significance |
| rs757009901 | 4:69,692,146 | G/T | — | uncertain significance |
| rs756068390 | 4:69,692,160 | T/A | — | uncertain significance |
| rs200803372 | 4:69,692,168 | G/A | — | uncertain significance |
| rs202159234 | 4:69,693,153 | A/C | — | uncertain significance |
| rs71616903 | 4:69,693,162 | T/C | — | likely benign |
| rs913826758 | 4:69,693,191 | C/T | — | uncertain significance |
| rs113958082 | 4:69,693,202 | G/A | — | uncertain significance |
| rs201775293 | 4:69,696,338 | A/G | — | uncertain significance |
| rs1201188777 | 4:69,696,404 | T/C | — | uncertain significance |
| rs375571968 | 4:69,696,413 | G/A | — | uncertain significance |
| rs571769543 | 4:69,696,433 | C/G | — | uncertain significance |
| rs777647804 | 4:69,696,449 | A/G | — | uncertain significance |
| rs112561475 | 4:69,696,451 | A/G | missense variant | — |
| rs2109708065 | 4:69,696,502 | G/T | — | uncertain significance |
| rs776024737 | 4:69,696,553 | T/C | — | uncertain significance |
| rs2529373247 | 4:69,696,580 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.