SLC12A8
solute carrier family 12 member 8
Summary
This gene is thought to be a candidate for psoriasis susceptibility. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Sep 2010]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs771546073 | 3:124,802,759 | C/T | — | uncertain significance |
| rs776564193 | 3:124,802,786 | C/G | — | uncertain significance |
| rs780460449 | 3:124,802,799 | C/T | — | uncertain significance |
| rs771266464 | 3:124,802,831 | A/T | — | uncertain significance |
| rs373256263 | 3:124,802,835 | C/G | — | uncertain significance |
| rs201194975 | 3:124,802,861 | G/A | — | uncertain significance |
| rs754266251 | 3:124,802,873 | T/A | — | uncertain significance |
| rs367619170 | 3:124,807,187 | C/T | — | uncertain significance |
| rs201636734 | 3:124,810,295 | C/G | — | uncertain significance |
| rs766607584 | 3:124,810,304 | C/T | — | likely benign |
| rs3732498 | 3:124,810,307 | G/A | — | uncertain significance |
| rs1459746575 | 3:124,810,354 | G/T | — | uncertain significance |
| rs373528909 | 3:124,810,959 | C/T | — | uncertain significance |
| rs761656679 | 3:124,810,985 | A/G | — | uncertain significance |
| rs767580907 | 3:124,810,991 | G/A | — | uncertain significance |
| rs765973822 | 3:124,811,014 | T/A | — | uncertain significance |
| rs553956252 | 3:124,826,333 | C/T | — | uncertain significance |
| rs577293115 | 3:124,826,342 | G/A | — | uncertain significance |
| rs200535650 | 3:124,826,403 | C/T | — | uncertain significance |
| rs778092307 | 3:124,826,424 | T/C | — | uncertain significance |
| rs1939062383 | 3:124,826,467 | G/C | — | uncertain significance |
| rs1939063737 | 3:124,826,498 | G/T | — | uncertain significance |
| rs1939064073 | 3:124,826,508 | C/T | — | uncertain significance |
| rs1290642823 | 3:124,826,684 | C/T | — | uncertain significance |
| rs973947012 | 3:124,826,688 | G/T | — | uncertain significance |
| rs767643191 | 3:124,826,739 | C/T | — | uncertain significance |
| rs766218616 | 3:124,826,760 | C/T | — | uncertain significance |
| rs753657542 | 3:124,826,844 | C/T | — | likely benign |
| rs759673944 | 3:124,826,949 | C/T | — | uncertain significance |
| rs373242490 | 3:124,829,080 | T/C | — | uncertain significance |
| rs200851560 | 3:124,829,094 | C/T | — | uncertain significance |
| rs200808328 | 3:124,829,112 | C/T | — | uncertain significance |
| rs369148747 | 3:124,837,622 | T/C | — | uncertain significance |
| rs2472448779 | 3:124,837,642 | G/A | — | uncertain significance |
| rs766951277 | 3:124,839,519 | C/T | — | uncertain significance |
| rs371758667 | 3:124,854,563 | G/A | — | uncertain significance |
| rs11925247 | 3:124,861,442 | A/T | regulatory region variant | — |
| rs11917613 | 3:124,861,521 | C/T | regulatory region variant | — |
| rs816328 | 3:124,882,267 | C/G | — | — |
| rs816329 | 3:124,882,278 | C/T | intron variant | — |
| rs2472534331 | 3:124,896,629 | T/G | — | uncertain significance |
| rs565606261 | 3:124,896,635 | C/G | — | uncertain significance |
| rs147013897 | 3:124,896,667 | C/T | — | uncertain significance |
| rs780279352 | 3:124,896,721 | G/A | — | uncertain significance |
| rs754173297 | 3:124,896,725 | C/G | — | uncertain significance |
| rs750892503 | 3:124,896,736 | C/T | — | uncertain significance |
| rs200031423 | 3:124,896,755 | C/T | — | likely benign |
| rs781046992 | 3:124,906,109 | G/T | — | uncertain significance |
| rs1934810348 | 3:124,906,124 | C/G | — | uncertain significance |
| rs200999644 | 3:124,906,136 | G/A | — | uncertain significance |
| rs372342126 | 3:124,906,146 | T/C | — | uncertain significance |
| rs775399116 | 3:124,906,155 | C/A | — | uncertain significance |
| rs376320288 | 3:124,906,161 | C/T | — | uncertain significance |
| rs34985183 | 3:124,906,162 | A/G | — | uncertain significance |
| rs924707648 | 3:124,906,178 | C/T | — | likely benign |
| rs375202810 | 3:124,906,208 | G/A | — | uncertain significance |
| rs1166656984 | 3:124,906,220 | A/G | — | uncertain significance |
| rs988209300 | 3:124,909,242 | A/C | — | uncertain significance |
| rs182887928 | 3:124,909,281 | A/T | — | uncertain significance |
| rs1043331212 | 3:124,909,317 | A/T | — | uncertain significance |
| rs941175025 | 3:124,909,340 | C/A | — | uncertain significance |
| rs200467361 | 3:124,909,355 | G/C | — | uncertain significance |
| rs12497133 | 3:124,921,920 | G/A | intron variant | — |
| rs5852449 | 3:124,927,668 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.