TAS1R2
taste 1 receptor member 2
Summary
Contributes to sweet taste receptor activity. Involved in detection of chemical stimulus involved in sensory perception of sweet taste and positive regulation of cytokinesis. Part of sweet taste receptor complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants85 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs138805955 | 1:19,166,161 | A/G | — | uncertain significance |
| rs762498954 | 1:19,166,245 | T/A | — | uncertain significance |
| rs760329980 | 1:19,166,260 | C/T | — | uncertain significance |
| rs147439926 | 1:19,166,276 | G/C | — | uncertain significance |
| rs748655290 | 1:19,166,293 | C/T | — | likely benign |
| rs751789754 | 1:19,166,371 | T/C | — | uncertain significance |
| rs116173086 | 1:19,166,378 | G/A | — | benign |
| rs768315702 | 1:19,166,439 | C/T | — | uncertain significance |
| rs776315177 | 1:19,166,440 | G/A | — | uncertain significance |
| rs143659721 | 1:19,166,479 | C/T | — | uncertain significance |
| rs2522422557 | 1:19,166,511 | C/T | — | uncertain significance |
| rs149445409 | 1:19,166,514 | G/A | — | uncertain significance |
| rs1199553808 | 1:19,166,578 | A/C | — | uncertain significance |
| rs2100504242 | 1:19,166,580 | G/T | — | uncertain significance |
| rs745788077 | 1:19,166,623 | G/A | — | uncertain significance |
| rs41273165 | 1:19,166,665 | C/T | — | uncertain significance |
| rs558866117 | 1:19,166,716 | G/C | — | uncertain significance |
| rs968855809 | 1:19,166,749 | C/T | — | uncertain significance |
| rs762907945 | 1:19,166,814 | C/A | — | uncertain significance |
| rs769808801 | 1:19,166,820 | G/A | — | uncertain significance |
| rs749503611 | 1:19,166,842 | A/T | — | uncertain significance |
| rs772527483 | 1:19,166,871 | A/G | — | uncertain significance |
| rs373796920 | 1:19,166,914 | T/C | — | uncertain significance |
| rs948155839 | 1:19,166,924 | C/A | — | uncertain significance |
| rs554678930 | 1:19,166,953 | G/A | — | uncertain significance |
| rs1479959674 | 1:19,166,967 | G/A | — | uncertain significance |
| rs150544987 | 1:19,166,989 | C/T | — | uncertain significance |
| rs201628216 | 1:19,167,003 | G/T | — | uncertain significance |
| rs2522426102 | 1:19,167,012 | T/G | — | uncertain significance |
| rs2522426215 | 1:19,167,016 | A/T | — | uncertain significance |
| rs3935570 | 1:19,167,371 | G/T | intron variant | — |
| rs766687403 | 1:19,168,246 | C/T | — | uncertain significance |
| rs2522430164 | 1:19,168,310 | C/T | — | uncertain significance |
| rs2522430206 | 1:19,168,322 | T/C | — | uncertain significance |
| rs115820797 | 1:19,168,354 | G/A | — | benign |
| rs145591806 | 1:19,175,847 | G/A | — | likely benign |
| rs140426137 | 1:19,175,875 | T/G | — | uncertain significance |
| rs565839301 | 1:19,175,884 | C/T | — | uncertain significance |
| rs201352113 | 1:19,175,900 | A/G | — | uncertain significance |
| rs143077243 | 1:19,175,909 | C/T | — | likely benign |
| rs145389646 | 1:19,175,933 | G/A | — | uncertain significance |
| rs767092035 | 1:19,175,936 | C/T | — | uncertain significance |
| rs752345369 | 1:19,175,945 | A/G | — | uncertain significance |
| rs35775756 | 1:19,175,973 | G/A | — | benign |
| rs2522449278 | 1:19,176,040 | A/G | — | uncertain significance |
| rs4920566 | 1:19,179,824 | A/G | intron variant | — |
| rs2522462307 | 1:19,180,795 | G/A | — | uncertain significance |
| rs762905857 | 1:19,180,874 | C/T | — | uncertain significance |
| rs1187001294 | 1:19,180,877 | A/C | — | uncertain significance |
| rs200472258 | 1:19,180,889 | A/G | — | uncertain significance |
| rs757678235 | 1:19,180,924 | G/A | — | uncertain significance |
| rs370068569 | 1:19,180,949 | G/A | — | uncertain significance |
| rs775440208 | 1:19,180,975 | A/G | — | uncertain significance |
| rs549094114 | 1:19,181,060 | C/T | — | uncertain significance |
| rs201197024 | 1:19,181,066 | C/T | — | uncertain significance |
| rs149739674 | 1:19,181,075 | C/T | — | uncertain significance |
| rs1476026047 | 1:19,181,078 | C/A | — | uncertain significance |
| rs371767994 | 1:19,181,100 | C/G | — | likely benign |
| rs1049098348 | 1:19,181,103 | C/G | — | uncertain significance |
| rs779846899 | 1:19,181,137 | G/C | — | uncertain significance |
| rs140330444 | 1:19,181,279 | G/A | — | uncertain significance |
| rs777052368 | 1:19,181,287 | C/T | — | uncertain significance |
| rs369617128 | 1:19,181,327 | C/T | — | uncertain significance |
| rs371978810 | 1:19,181,328 | G/T | — | uncertain significance |
| rs200290887 | 1:19,181,336 | C/G | — | uncertain significance |
| rs138816008 | 1:19,181,365 | T/C | — | uncertain significance |
| rs758466636 | 1:19,181,390 | C/T | — | uncertain significance |
| rs35874116 | 1:19,181,393 | A/G | missense variant | — |
| rs778307315 | 1:19,181,402 | C/T | — | uncertain significance |
| rs536515901 | 1:19,181,419 | C/T | — | uncertain significance |
| rs755156769 | 1:19,181,431 | G/A | — | uncertain significance |
| rs756517501 | 1:19,181,438 | G/C | — | uncertain significance |
| rs749792975 | 1:19,181,447 | C/G | — | uncertain significance |
| rs1265607836 | 1:19,183,866 | T/C | — | uncertain significance |
| rs776534722 | 1:19,184,013 | C/T | — | uncertain significance |
| rs376502751 | 1:19,184,036 | C/T | — | likely benign |
| rs764869881 | 1:19,184,046 | G/C | — | uncertain significance |
| rs111534973 | 1:19,184,075 | G/A | — | uncertain significance |
| rs199501438 | 1:19,184,082 | G/A | — | uncertain significance |
| rs774804541 | 1:19,184,105 | C/A | — | uncertain significance |
| rs2522479124 | 1:19,186,040 | A/C | — | uncertain significance |
| rs1010731174 | 1:19,186,083 | G/C | — | uncertain significance |
| rs72953144 | 1:19,186,093 | G/A | — | benign |
| rs139685223 | 1:19,186,115 | G/C | — | uncertain significance |
| rs9701796 | 1:19,186,129 | G/C | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.