TAAR2
trace amine associated receptor 2
Summary
Predicted to enable trace-amine receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1444823600 | 6:132,938,320 | G/T | — | uncertain significance |
| rs2483189362 | 6:132,938,333 | A/G | — | uncertain significance |
| rs200471202 | 6:132,938,402 | A/G | — | uncertain significance |
| rs372803383 | 6:132,938,403 | T/C | — | uncertain significance |
| rs746705772 | 6:132,938,410 | G/A | — | uncertain significance |
| rs1296881171 | 6:132,938,486 | A/G | — | uncertain significance |
| rs746428524 | 6:132,938,573 | T/G | — | uncertain significance |
| rs772848812 | 6:132,938,605 | C/T | — | uncertain significance |
| rs375499103 | 6:132,938,614 | T/C | — | uncertain significance |
| rs368292716 | 6:132,938,616 | G/C | — | uncertain significance |
| rs376107701 | 6:132,938,629 | T/C | — | uncertain significance |
| rs1237920142 | 6:132,938,669 | C/T | — | uncertain significance |
| rs770782356 | 6:132,938,677 | G/T | — | uncertain significance |
| rs61731217 | 6:132,938,687 | T/C | — | uncertain significance |
| rs1378899435 | 6:132,938,703 | A/C | — | uncertain significance |
| rs751950255 | 6:132,938,734 | A/G | — | uncertain significance |
| rs141239990 | 6:132,938,812 | A/T | — | uncertain significance |
| rs142577385 | 6:132,938,938 | G/A | — | uncertain significance |
| rs773819525 | 6:132,938,963 | T/C | — | uncertain significance |
| rs369503456 | 6:132,939,010 | C/T | — | uncertain significance |
| rs550125345 | 6:132,939,034 | G/C | — | uncertain significance |
| rs2483192936 | 6:132,939,044 | T/C | — | uncertain significance |
| rs1389203364 | 6:132,939,187 | G/A | — | uncertain significance |
| rs202050977 | 6:132,939,212 | C/T | — | uncertain significance |
| rs201583865 | 6:132,939,230 | A/G | — | likely benign |
| rs140760185 | 6:132,944,498 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.