SLC12A9
solute carrier family 12 member 9
Summary
Predicted to enable potassium:chloride symporter activity. Predicted to be involved in several processes, including chloride ion homeostasis; chloride transmembrane transport; and potassium ion homeostasis. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs192023252 | 7:100,438,964 | C/G | intron variant | — |
| rs314332 | 7:100,443,960 | G/T | — | — |
| rs531230000 | 7:100,447,651 | C/T | — | — |
| rs138395732 | 7:100,449,133 | C/T | upstream gene variant | — |
| rs760173586 | 7:100,451,854 | G/A | — | uncertain significance |
| rs374596888 | 7:100,452,246 | C/G | — | uncertain significance |
| rs368327144 | 7:100,452,322 | C/A | — | uncertain significance |
| rs767234195 | 7:100,452,370 | G/A | — | uncertain significance |
| rs314370 | 7:100,453,208 | T/A | — | — |
| rs376562429 | 7:100,453,436 | C/G | — | uncertain significance |
| rs753771086 | 7:100,453,439 | T/C | — | uncertain significance |
| rs138890264 | 7:100,453,456 | G/A | — | uncertain significance |
| rs143663491 | 7:100,454,513 | C/T | — | uncertain significance |
| rs1814443263 | 7:100,454,735 | C/G | — | uncertain significance |
| rs771524495 | 7:100,454,742 | C/T | — | uncertain significance |
| rs530739144 | 7:100,456,475 | A/C | — | uncertain significance |
| rs78261122 | 7:100,456,506 | C/T | — | benign |
| rs314373 | 7:100,456,595 | G/A | intron variant | — |
| rs144447119 | 7:100,456,711 | C/T | — | uncertain significance |
| rs371521867 | 7:100,456,716 | G/A | — | likely benign |
| rs142969838 | 7:100,456,725 | G/A | — | uncertain significance |
| rs2485170538 | 7:100,457,519 | G/C | — | uncertain significance |
| rs80308281 | 7:100,457,578 | T/C | missense variant | — |
| rs149149897 | 7:100,457,623 | C/T | — | uncertain significance |
| rs749151870 | 7:100,457,777 | A/G | — | uncertain significance |
| rs367880579 | 7:100,457,783 | G/A | — | uncertain significance |
| rs7801190 | 7:100,458,093 | C/G | intron variant | — |
| rs959025951 | 7:100,458,827 | A/G | — | uncertain significance |
| rs200508321 | 7:100,458,835 | G/A | — | uncertain significance |
| rs763724101 | 7:100,459,093 | C/T | — | uncertain significance |
| rs199820283 | 7:100,459,100 | C/T | — | uncertain significance |
| rs749375754 | 7:100,459,138 | G/A | — | uncertain significance |
| rs146848048 | 7:100,459,467 | C/T | — | uncertain significance |
| rs538145183 | 7:100,459,468 | G/A | — | uncertain significance |
| rs777752368 | 7:100,459,491 | G/T | — | uncertain significance |
| rs745538841 | 7:100,459,495 | G/T | — | uncertain significance |
| rs1264920700 | 7:100,459,507 | T/A | — | uncertain significance |
| rs1479003611 | 7:100,459,518 | A/G | — | uncertain significance |
| rs757933227 | 7:100,460,357 | T/C | — | uncertain significance |
| rs117717323 | 7:100,461,690 | C/T | upstream gene variant | — |
| rs374398396 | 7:100,463,392 | C/T | — | uncertain significance |
| rs201536686 | 7:100,463,410 | C/T | — | uncertain significance |
| rs756159689 | 7:100,463,503 | G/T | — | uncertain significance |
| rs778829948 | 7:100,463,530 | A/G | — | uncertain significance |
| rs2485227008 | 7:100,463,589 | A/C | — | uncertain significance |
| rs758283919 | 7:100,463,607 | G/C | — | uncertain significance |
| rs199572979 | 7:100,463,619 | C/T | — | uncertain significance |
| rs767897795 | 7:100,463,622 | G/C | — | uncertain significance |
| rs1249228582 | 7:100,463,686 | G/A | — | uncertain significance |
| rs145941674 | 7:100,463,775 | C/T | — | uncertain significance |
| rs756083425 | 7:100,463,782 | G/A | — | uncertain significance |
| rs200771346 | 7:100,463,802 | C/A | — | uncertain significance |
| rs770485080 | 7:100,463,806 | G/A | — | likely benign |
| rs778633195 | 7:100,463,812 | C/T | — | uncertain significance |
| rs200018649 | 7:100,463,832 | C/T | — | uncertain significance |
| rs202174092 | 7:100,463,839 | G/A | — | uncertain significance |
| rs745568147 | 7:100,463,866 | G/A | — | uncertain significance |
| rs771390111 | 7:100,464,006 | C/T | — | uncertain significance |
| rs746002049 | 7:100,464,022 | G/A | — | uncertain significance |
| rs779291642 | 7:100,464,135 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.