GPR20
G protein-coupled receptor 20
Summary
Enables G protein-coupled receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Located in plasma membrane. Part of receptor complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs371086797 | 8:142,366,985 | C/T | — | uncertain significance |
| rs143127247 | 8:142,366,986 | G/A | — | benign |
| rs750645239 | 8:142,367,051 | C/T | — | likely benign |
| rs201855453 | 8:142,367,078 | C/T | — | uncertain significance |
| rs765079608 | 8:142,367,098 | C/T | — | uncertain significance |
| rs559578522 | 8:142,367,102 | C/T | — | uncertain significance |
| rs201448608 | 8:142,367,195 | C/T | — | uncertain significance |
| rs141443646 | 8:142,367,221 | G/T | — | uncertain significance |
| rs36092215 | 8:142,367,246 | G/A | missense variant | — |
| rs201478564 | 8:142,367,259 | C/T | — | likely benign |
| rs574585646 | 8:142,367,315 | C/G | — | uncertain significance |
| rs375656717 | 8:142,367,326 | C/T | — | uncertain significance |
| rs745885340 | 8:142,367,366 | T/C | — | likely benign |
| rs771739805 | 8:142,367,384 | C/T | — | uncertain significance |
| rs368685016 | 8:142,367,437 | C/T | — | uncertain significance |
| rs2537231881 | 8:142,367,444 | A/G | — | uncertain significance |
| rs551289725 | 8:142,367,489 | C/T | — | uncertain significance |
| rs2537232083 | 8:142,367,528 | A/T | — | uncertain significance |
| rs373481136 | 8:142,367,539 | C/T | — | uncertain significance |
| rs769778958 | 8:142,367,546 | G/A | — | uncertain significance |
| rs774005283 | 8:142,367,558 | C/T | — | uncertain significance |
| rs1284141969 | 8:142,367,599 | G/A | — | uncertain significance |
| rs150581192 | 8:142,367,603 | G/A | — | uncertain significance |
| rs371640941 | 8:142,367,663 | G/A | — | uncertain significance |
| rs369261216 | 8:142,367,689 | A/G | — | uncertain significance |
| rs545713038 | 8:142,367,693 | C/T | — | uncertain significance |
| rs1396168257 | 8:142,367,773 | G/A | — | uncertain significance |
| rs374341766 | 8:142,367,795 | C/T | — | uncertain significance |
| rs201753029 | 8:142,367,828 | C/T | — | uncertain significance |
| rs143776711 | 8:142,367,850 | C/T | — | likely benign |
| rs533635492 | 8:142,367,905 | C/T | — | uncertain significance |
| rs1346298161 | 8:142,367,945 | C/T | — | uncertain significance |
| rs377253856 | 8:142,367,950 | G/A | — | uncertain significance |
| rs370443305 | 8:142,367,953 | C/T | — | uncertain significance |
| rs2537233472 | 8:142,367,960 | T/A | — | uncertain significance |
| rs549200262 | 8:142,367,969 | C/T | — | uncertain significance |
| rs768592430 | 8:142,367,990 | C/T | — | uncertain significance |
| rs149500874 | 8:142,367,999 | G/A | — | uncertain significance |
| rs112529921 | 8:142,368,001 | C/A | — | uncertain significance |
| rs748344567 | 8:142,368,018 | G/C | — | likely benign |
| rs56251106 | 8:142,374,304 | C/T | — | — |
| rs78192203 | 8:142,375,073 | T/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.