SLC22A23
solute carrier family 22 member 23
Summary
SLC22A23 belongs to a large family of transmembrane proteins that function as uniporters, symporters, and antiporters to transport organic ions across cell membranes (Jacobsson et al., 2007 [PubMed 17714910]).[supplied by OMIM, Mar 2008]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs760054804 | 6:3,273,303 | T/A | — | uncertain significance |
| rs777308990 | 6:3,273,345 | C/G | — | uncertain significance |
| rs1189427628 | 6:3,273,371 | T/C | — | uncertain significance |
| rs141223516 | 6:3,273,419 | T/G | — | uncertain significance |
| rs924660068 | 6:3,273,453 | C/T | — | uncertain significance |
| rs141353043 | 6:3,273,613 | C/T | — | likely benign |
| rs35042900 | 6:3,273,616 | G/A | — | benign |
| rs4479984 | 6:3,281,205 | G/T | intron variant | — |
| rs114632171 | 6:3,284,094 | C/G | — | likely benign |
| rs199958017 | 6:3,284,103 | G/C | — | uncertain significance |
| rs149762554 | 6:3,284,174 | C/T | — | likely benign |
| rs745493017 | 6:3,284,205 | C/T | — | uncertain significance |
| rs148573369 | 6:3,285,317 | G/T | — | uncertain significance |
| rs2480335641 | 6:3,285,331 | T/A | — | uncertain significance |
| rs768978485 | 6:3,290,056 | C/T | — | uncertain significance |
| rs762038656 | 6:3,290,059 | T/C | — | uncertain significance |
| rs1022251534 | 6:3,290,080 | G/A | — | uncertain significance |
| rs9378357 | 6:3,294,824 | G/T | intron variant | — |
| rs757839112 | 6:3,298,433 | G/A | — | uncertain significance |
| rs9391988 | 6:3,307,863 | G/A | downstream gene variant | — |
| rs567050291 | 6:3,316,091 | C/A | — | — |
| rs760194361 | 6:3,324,084 | T/C | — | uncertain significance |
| rs766850904 | 6:3,324,131 | C/T | — | uncertain significance |
| rs376011377 | 6:3,324,210 | G/A | — | uncertain significance |
| rs4959235 | 6:3,359,337 | T/C | intron variant | — |
| rs6922506 | 6:3,362,059 | C/A | regulatory region variant | — |
| rs9391993 | 6:3,369,509 | G/A | — | — |
| rs370166164 | 6:3,410,440 | G/C | — | uncertain significance |
| rs374183830 | 6:3,410,473 | A/C | — | uncertain significance |
| rs2481375764 | 6:3,410,474 | C/A | — | uncertain significance |
| rs1327218910 | 6:3,410,536 | T/C | — | uncertain significance |
| rs781179173 | 6:3,410,565 | C/T | — | uncertain significance |
| rs61614579 | 6:3,423,547 | T/G | intron variant | — |
| rs58167401 | 6:3,423,587 | A/C | intron variant | — |
| rs17309827 | 6:3,433,318 | T/G | regulatory region variant | — |
| rs112136863 | 6:3,439,358 | G/A | intron variant | — |
| rs9503599 | 6:3,451,048 | T/C | intron variant | — |
| rs967582853 | 6:3,456,144 | C/T | — | uncertain significance |
| rs1049363326 | 6:3,456,178 | C/G | — | uncertain significance |
| rs774447303 | 6:3,456,204 | T/C | — | uncertain significance |
| rs762707895 | 6:3,456,346 | C/G | — | uncertain significance |
| rs913425998 | 6:3,456,347 | C/A | — | uncertain significance |
| rs779155487 | 6:3,456,402 | G/A | — | uncertain significance |
| rs754494830 | 6:3,456,532 | G/A | — | uncertain significance |
| rs953820416 | 6:3,456,666 | C/T | — | uncertain significance |
| rs1772413940 | 6:3,456,676 | C/T | — | uncertain significance |
| rs2481736093 | 6:3,456,687 | G/C | — | uncertain significance |
| rs972769483 | 6:3,456,754 | G/A | — | uncertain significance |
| rs2481737124 | 6:3,456,780 | C/T | — | uncertain significance |
| rs1048250379 | 6:3,456,787 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.