SLC6A12
solute carrier family 6 member 12
Summary
Enables gamma-aminobutyric acid:sodium:chloride symporter activity. Involved in gamma-aminobutyric acid transport and monocarboxylic acid transport. Predicted to be located in basolateral plasma membrane. Predicted to be active in cell projection and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11061809 | 12:293,773 | G/C | upstream gene variant | — |
| rs372692550 | 12:300,241 | T/G | — | uncertain significance |
| rs141965662 | 12:300,257 | C/T | — | uncertain significance |
| rs750197629 | 12:300,262 | A/G | — | uncertain significance |
| rs537332809 | 12:300,298 | C/T | — | likely benign |
| rs976658726 | 12:300,326 | G/A | — | uncertain significance |
| rs143357433 | 12:301,685 | C/T | — | likely benign |
| rs75000134 | 12:301,749 | C/T | — | benign |
| rs563357289 | 12:301,763 | C/T | — | likely benign |
| rs1339474064 | 12:302,459 | G/T | — | uncertain significance |
| rs138178078 | 12:302,492 | C/G | — | likely benign |
| rs141848384 | 12:302,499 | G/A | — | uncertain significance |
| rs115223250 | 12:305,281 | G/C | — | benign |
| rs375791935 | 12:305,328 | C/G | — | uncertain significance |
| rs766025879 | 12:305,355 | G/A | — | uncertain significance |
| rs149207141 | 12:305,369 | C/T | — | uncertain significance |
| rs140265072 | 12:305,406 | C/T | — | uncertain significance |
| rs2497689717 | 12:305,938 | G/C | — | uncertain significance |
| rs2497690596 | 12:306,022 | G/A | — | uncertain significance |
| rs151111165 | 12:306,028 | C/T | — | uncertain significance |
| rs761912292 | 12:306,045 | G/A | — | uncertain significance |
| rs747692783 | 12:306,624 | C/T | — | uncertain significance |
| rs1409260606 | 12:307,156 | G/A | — | uncertain significance |
| rs115308035 | 12:307,167 | C/T | — | benign |
| rs74057609 | 12:308,077 | C/A | — | benign |
| rs781320561 | 12:309,900 | G/A | — | uncertain significance |
| rs547529730 | 12:309,926 | G/A | — | uncertain significance |
| rs112982618 | 12:313,785 | T/C | — | benign |
| rs761222307 | 12:313,816 | G/A | — | uncertain significance |
| rs1940531332 | 12:313,843 | A/C | — | uncertain significance |
| rs2300125 | 12:315,390 | C/T | downstream gene variant | — |
| rs374785609 | 12:318,945 | C/T | — | uncertain significance |
| rs371007985 | 12:319,067 | T/A | — | uncertain significance |
| rs150191926 | 12:319,124 | C/G | — | uncertain significance |
| rs557881 | 12:319,125 | A/G | missense variant | — |
| rs768581304 | 12:319,128 | C/T | — | uncertain significance |
| rs372181092 | 12:319,130 | T/C | — | uncertain significance |
| rs499368 | 12:320,920 | T/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.