SLC6A13
solute carrier family 6 member 13
Summary
Enables gamma-aminobutyric acid:sodium:chloride symporter activity. Involved in amino acid import across plasma membrane and monocarboxylic acid transport. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201412174 | 12:330,179 | G/T | — | uncertain significance |
| rs146023208 | 12:330,194 | G/A | — | uncertain significance |
| rs537041083 | 12:330,230 | G/A | — | uncertain significance |
| rs116358772 | 12:330,535 | G/A | — | benign |
| rs1310408845 | 12:330,557 | C/A | — | uncertain significance |
| rs201412499 | 12:330,613 | G/C | — | uncertain significance |
| rs752824610 | 12:330,648 | G/A | — | uncertain significance |
| rs2497899749 | 12:331,732 | T/G | — | uncertain significance |
| rs139777154 | 12:331,789 | C/T | — | uncertain significance |
| rs1269693402 | 12:332,303 | A/G | — | uncertain significance |
| rs369427960 | 12:332,325 | C/T | — | uncertain significance |
| rs771936006 | 12:332,326 | G/T | — | uncertain significance |
| rs142303290 | 12:332,338 | G/A | — | benign |
| rs147044076 | 12:332,397 | C/T | — | uncertain significance |
| rs182480724 | 12:333,184 | G/T | — | uncertain significance |
| rs370762914 | 12:333,201 | A/G | — | uncertain significance |
| rs145646067 | 12:333,225 | C/T | — | benign |
| rs16928571 | 12:333,245 | G/A | — | benign |
| rs138250879 | 12:333,248 | A/G | — | benign |
| rs148015114 | 12:333,289 | A/G | — | uncertain significance |
| rs753022537 | 12:333,583 | A/G | — | uncertain significance |
| rs145951312 | 12:333,591 | G/A | — | likely benign |
| rs779439486 | 12:333,598 | A/C | — | uncertain significance |
| rs149299701 | 12:333,650 | G/A | — | uncertain significance |
| rs73038087 | 12:334,844 | G/A | intron variant | — |
| rs76709380 | 12:335,578 | G/C | — | benign |
| rs536955832 | 12:335,649 | C/T | — | uncertain significance |
| rs1326399746 | 12:335,676 | A/G | — | uncertain significance |
| rs555044 | 12:335,922 | C/A | regulatory region variant | — |
| rs780979529 | 12:336,737 | C/T | — | uncertain significance |
| rs373477459 | 12:336,795 | C/T | — | uncertain significance |
| rs2497930352 | 12:336,804 | A/G | — | uncertain significance |
| rs777167331 | 12:336,807 | A/G | — | uncertain significance |
| rs1236167026 | 12:344,258 | G/C | — | uncertain significance |
| rs142344531 | 12:344,275 | G/A | — | uncertain significance |
| rs756606932 | 12:344,341 | A/G | — | uncertain significance |
| rs562454555 | 12:344,362 | T/C | — | uncertain significance |
| rs373279173 | 12:346,406 | C/T | — | uncertain significance |
| rs2289957 | 12:347,068 | T/C | — | — |
| rs2497991209 | 12:347,091 | C/T | — | likely pathogenic |
| rs765557068 | 12:347,108 | C/G | — | uncertain significance |
| rs777433614 | 12:347,122 | T/C | — | uncertain significance |
| rs67523949 | 12:348,506 | C/T | intron variant | — |
| rs10774020 | 12:348,876 | T/C | intron variant | — |
| rs10774021 | 12:349,298 | C/T | intron variant | — |
| rs11613331 | 12:351,467 | G/A | intron variant | — |
| rs1375831288 | 12:351,866 | A/G | — | uncertain significance |
| rs369072954 | 12:351,894 | C/T | — | uncertain significance |
| rs1197612180 | 12:351,917 | A/G | — | uncertain significance |
| rs779328529 | 12:351,918 | T/C | — | uncertain significance |
| rs2498019060 | 12:352,929 | C/T | — | uncertain significance |
| rs147275386 | 12:352,956 | C/T | — | likely benign |
| rs7969761 | 12:355,842 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.