SLC22A3
solute carrier family 22 member 3
Summary
Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. [provided by RefSeq, Jul 2008]
Known Variants89 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs551032 | 6:160,768,860 | T/C | regulatory region variant | — |
| rs555754 | 6:160,769,423 | G/A | — | benign |
| rs2114922463 | 6:160,769,483 | T/C | — | likely benign |
| rs1784547551 | 6:160,769,567 | T/C | — | uncertain significance |
| rs1177376771 | 6:160,769,620 | G/A | — | uncertain significance |
| rs772653083 | 6:160,769,632 | G/C | — | uncertain significance |
| rs769378803 | 6:160,769,655 | G/C | — | uncertain significance |
| rs2114923014 | 6:160,769,683 | T/C | — | uncertain significance |
| rs768140693 | 6:160,769,684 | C/G | — | uncertain significance |
| rs1784554194 | 6:160,769,687 | G/T | — | uncertain significance |
| rs1052623749 | 6:160,769,698 | C/T | — | uncertain significance |
| rs1583431592 | 6:160,769,709 | C/G | — | likely benign |
| rs1469600200 | 6:160,769,737 | G/C | — | uncertain significance |
| rs41267799 | 6:160,770,018 | C/G | — | — |
| rs541091 | 6:160,770,552 | G/A | regulatory region variant | — |
| rs639426 | 6:160,771,766 | G/A | intron variant | — |
| rs637614 | 6:160,772,133 | T/C | intron variant | — |
| rs34790642 | 6:160,772,611 | A/G | — | — |
| rs577392387 | 6:160,772,624 | A/C | — | — |
| rs609562 | 6:160,773,819 | T/C | intron variant | — |
| rs486359 | 6:160,774,441 | G/A | — | — |
| rs563015690 | 6:160,774,572 | T/C | — | — |
| rs416879 | 6:160,774,838 | A/T | — | — |
| rs512077 | 6:160,774,928 | A/G | intron variant | — |
| rs529913906 | 6:160,775,006 | G/A | — | — |
| rs695174 | 6:160,775,510 | G/A | intron variant | — |
| rs759659447 | 6:160,775,803 | C/T | — | — |
| rs673736 | 6:160,776,653 | G/A | intron variant | — |
| rs150740982 | 6:160,777,718 | C/T | intron variant | — |
| rs140078298 | 6:160,779,991 | A/T | intron variant | — |
| rs9364552 | 6:160,782,934 | G/T | — | — |
| rs187044063 | 6:160,786,631 | T/G | intron variant | — |
| rs402219 | 6:160,789,296 | A/G | intron variant | — |
| rs3127574 | 6:160,791,370 | C/T | — | — |
| rs12204009 | 6:160,799,246 | T/C | regulatory region variant | — |
| rs149302195 | 6:160,803,694 | C/T | intron variant | — |
| rs144579839 | 6:160,804,264 | G/A | intron variant | — |
| rs420038 | 6:160,808,148 | C/T | regulatory region variant | benign |
| rs555049314 | 6:160,810,079 | C/T | — | — |
| rs184465278 | 6:160,818,614 | A/C | intron variant | — |
| rs775845108 | 6:160,819,020 | G/C | — | uncertain significance |
| rs201505818 | 6:160,819,038 | A/C | — | uncertain significance |
| rs2504916 | 6:160,824,028 | T/G | — | — |
| rs2504938 | 6:160,824,754 | C/T | coding sequence variant | — |
| rs778599126 | 6:160,828,173 | C/T | — | uncertain significance |
| rs974236516 | 6:160,828,189 | T/A | — | uncertain significance |
| rs371628612 | 6:160,828,191 | T/A | — | uncertain significance |
| rs201195713 | 6:160,829,803 | C/T | — | uncertain significance |
| rs368056298 | 6:160,829,829 | G/A | — | uncertain significance |
| rs1787126198 | 6:160,829,871 | G/A | — | uncertain significance |
| rs575539551 | 6:160,829,883 | T/C | — | uncertain significance |
| rs747240128 | 6:160,829,893 | A/G | — | uncertain significance |
| rs776119192 | 6:160,829,920 | C/T | — | uncertain significance |
| rs544366796 | 6:160,830,550 | C/G | — | — |
| rs1167977709 | 6:160,831,795 | C/T | — | uncertain significance |
| rs151135411 | 6:160,831,796 | G/A | missense variant | — |
| rs9364554 | 6:160,833,664 | C/T | intron variant | — |
| rs185226914 | 6:160,834,323 | G/T | regulatory region variant | — |
| rs2457571 | 6:160,834,828 | T/C | intron variant | — |
| rs1112444 | 6:160,835,192 | C/T | — | — |
| rs145846934 | 6:160,838,582 | A/G | intron variant | — |
| rs141463285 | 6:160,838,646 | T/A | intron variant | — |
| rs7758229 | 6:160,840,252 | G/A | — | — |
| rs529191541 | 6:160,853,562 | C/T | — | — |
| rs74907759 | 6:160,857,193 | A/G | intron variant | — |
| rs115325990 | 6:160,857,787 | A/G | intron variant | — |
| rs145328121 | 6:160,857,878 | A/T | — | uncertain significance |
| rs201627538 | 6:160,857,988 | A/C | intron variant | — |
| rs377738242 | 6:160,858,066 | C/A | — | uncertain significance |
| rs200861075 | 6:160,858,079 | T/G | — | uncertain significance |
| rs1326838516 | 6:160,858,087 | A/G | — | uncertain significance |
| rs369478939 | 6:160,858,157 | T/C | — | uncertain significance |
| rs145082363 | 6:160,858,175 | G/T | — | uncertain significance |
| rs2292334 | 6:160,858,188 | G/A | synonymous variant | benign |
| rs189821701 | 6:160,862,809 | C/T | intron variant | — |
| rs2048327 | 6:160,863,532 | T/C | intron variant | — |
| rs549975194 | 6:160,863,985 | C/T | — | — |
| rs8187722 | 6:160,864,758 | A/G | synonymous variant | — |
| rs961213755 | 6:160,864,759 | C/T | — | uncertain significance |
| rs1239258880 | 6:160,864,760 | C/T | — | uncertain significance |
| rs7769879 | 6:160,865,645 | G/C | intron variant | — |
| rs762813849 | 6:160,868,754 | T/C | — | uncertain significance |
| rs2483672746 | 6:160,868,839 | A/T | — | uncertain significance |
| rs145828284 | 6:160,869,957 | A/T | downstream gene variant | — |
| rs372635730 | 6:160,870,620 | G/A | — | — |
| rs866366948 | 6:160,872,051 | G/C | — | uncertain significance |
| rs1810126 | 6:160,872,151 | C/T | regulatory region variant | — |
| rs115069429 | 6:160,872,648 | T/C | downstream gene variant | — |
| rs3088442 | 6:160,872,652 | G/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.