FFAR3
free fatty acid receptor 3
Summary
Enables G protein-coupled receptor activity. Involved in adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway and cellular response to fatty acid. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10422744 | 19:35,847,153 | C/T | regulatory region variant | — |
| rs1353677437 | 19:35,849,796 | G/A | — | uncertain significance |
| rs1419147868 | 19:35,849,826 | G/C | — | uncertain significance |
| rs2513683126 | 19:35,849,832 | C/T | — | uncertain significance |
| rs62109581 | 19:35,849,926 | G/A | — | benign |
| rs1451058267 | 19:35,849,965 | C/A | — | uncertain significance |
| rs755812436 | 19:35,849,967 | G/A | — | uncertain significance |
| rs556917621 | 19:35,850,006 | A/G | — | uncertain significance |
| rs1359991796 | 19:35,850,012 | G/A | — | uncertain significance |
| rs2513683635 | 19:35,850,027 | A/G | — | uncertain significance |
| rs2513683641 | 19:35,850,029 | G/A | — | uncertain significance |
| rs764883825 | 19:35,850,043 | C/T | — | uncertain significance |
| rs773529515 | 19:35,850,099 | G/A | — | uncertain significance |
| rs775174456 | 19:35,850,129 | C/T | — | uncertain significance |
| rs373181049 | 19:35,850,139 | G/A | — | uncertain significance |
| rs530606489 | 19:35,850,237 | G/A | — | uncertain significance |
| rs147815439 | 19:35,850,246 | G/A | — | likely benign |
| rs772009363 | 19:35,850,288 | A/C | — | uncertain significance |
| rs2513684234 | 19:35,850,331 | T/A | — | uncertain significance |
| rs377320729 | 19:35,850,342 | G/A | — | uncertain significance |
| rs145113005 | 19:35,850,395 | C/T | — | likely benign |
| rs777343801 | 19:35,850,435 | G/T | — | uncertain significance |
| rs745314632 | 19:35,850,489 | A/T | — | uncertain significance |
| rs1247388515 | 19:35,850,498 | G/T | — | uncertain significance |
| rs148946992 | 19:35,850,556 | C/T | — | uncertain significance |
| rs375946 | 19:35,850,560 | G/A | — | likely benign |
| rs778870629 | 19:35,850,561 | T/C | — | uncertain significance |
| rs141433014 | 19:35,850,577 | C/T | — | likely benign |
| rs201374965 | 19:35,850,579 | C/T | — | uncertain significance |
| rs1786344879 | 19:35,850,649 | A/T | — | uncertain significance |
| rs756362529 | 19:35,850,687 | G/A | — | uncertain significance |
| rs780185794 | 19:35,850,688 | G/C | — | uncertain significance |
| rs150331058 | 19:35,850,711 | A/C | — | uncertain significance |
| rs137994496 | 19:35,850,752 | G/A | — | likely benign |
| rs10407548 | 19:35,851,615 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.