SLC16A6
solute carrier family 16 member 6
Summary
Predicted to enable monocarboxylic acid transmembrane transporter activity. Predicted to be involved in monocarboxylic acid transport. Predicted to be located in basolateral plasma membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs782052199 | 17:66,265,257 | C/T | — | likely benign |
| rs782242193 | 17:66,265,332 | G/A | — | uncertain significance |
| rs1555748247 | 17:66,266,991 | G/A | — | uncertain significance |
| rs782595962 | 17:66,267,205 | C/T | — | uncertain significance |
| rs782234985 | 17:66,267,357 | A/C | — | uncertain significance |
| rs2075329771 | 17:66,267,370 | G/A | — | uncertain significance |
| rs543240847 | 17:66,267,397 | G/T | — | uncertain significance |
| rs112262188 | 17:66,267,485 | G/C | — | benign |
| rs2509702013 | 17:66,267,567 | G/A | — | uncertain significance |
| rs61745585 | 17:66,267,606 | C/T | — | uncertain significance |
| rs1168203877 | 17:66,267,625 | G/C | — | uncertain significance |
| rs781980063 | 17:66,267,636 | G/A | — | likely benign |
| rs377560800 | 17:66,267,645 | C/T | — | uncertain significance |
| rs370502404 | 17:66,267,654 | T/C | — | uncertain significance |
| rs367677855 | 17:66,267,720 | A/C | — | uncertain significance |
| rs144470811 | 17:66,267,724 | T/C | — | uncertain significance |
| rs61740584 | 17:66,267,734 | T/C | — | benign |
| rs62087130 | 17:66,267,752 | G/A | — | likely benign |
| rs1555749368 | 17:66,268,801 | C/T | — | uncertain significance |
| rs1164626510 | 17:66,268,824 | A/G | — | uncertain significance |
| rs2509716503 | 17:66,268,902 | C/T | — | uncertain significance |
| rs782407139 | 17:66,270,086 | C/T | — | likely benign |
| rs557032590 | 17:66,270,094 | A/G | — | uncertain significance |
| rs112872270 | 17:66,270,110 | G/T | — | uncertain significance |
| rs142630255 | 17:66,270,179 | C/T | — | uncertain significance |
| rs2075584722 | 17:66,274,283 | T/C | — | uncertain significance |
| rs139353004 | 17:66,274,298 | C/G | — | uncertain significance |
| rs2509764928 | 17:66,274,377 | C/T | — | uncertain significance |
| rs782672096 | 17:66,274,424 | T/C | — | uncertain significance |
| rs143508642 | 17:66,278,442 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.