ADGRG7
adhesion G protein-coupled receptor G7
Summary
Predicted to enable G protein-coupled receptor activity. Predicted to be involved in adenylate cyclase-activating 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 Variants63 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs72914695 | 3:100,328,733 | G/C | — | benign |
| rs140472196 | 3:100,328,764 | G/T | — | uncertain significance |
| rs367805466 | 3:100,349,588 | T/C | — | uncertain significance |
| rs1315251758 | 3:100,349,635 | G/A | — | uncertain significance |
| rs200895145 | 3:100,352,109 | C/T | — | uncertain significance |
| rs1707481210 | 3:100,352,121 | T/C | — | uncertain significance |
| rs369393091 | 3:100,352,129 | C/T | — | uncertain significance |
| rs143646459 | 3:100,352,130 | G/A | — | uncertain significance |
| rs1431767477 | 3:100,352,217 | A/G | — | uncertain significance |
| rs767048784 | 3:100,354,596 | A/G | — | uncertain significance |
| rs190503505 | 3:100,354,621 | C/T | — | uncertain significance |
| rs780049267 | 3:100,356,230 | G/T | — | uncertain significance |
| rs41272971 | 3:100,362,114 | A/G | — | uncertain significance |
| rs376767128 | 3:100,362,115 | T/C | — | uncertain significance |
| rs1707676549 | 3:100,362,159 | G/C | — | uncertain significance |
| rs774786770 | 3:100,362,162 | G/C | — | uncertain significance |
| rs751437270 | 3:100,362,197 | C/A | — | uncertain significance |
| rs779730760 | 3:100,362,231 | C/T | — | uncertain significance |
| rs375365345 | 3:100,362,363 | C/T | — | likely benign |
| rs1194076848 | 3:100,362,405 | A/G | — | likely benign |
| rs2472333408 | 3:100,364,799 | G/T | — | uncertain significance |
| rs756292338 | 3:100,364,819 | A/G | — | uncertain significance |
| rs139133596 | 3:100,364,833 | C/G | — | uncertain significance |
| rs779095865 | 3:100,364,864 | C/T | — | uncertain significance |
| rs2472333594 | 3:100,364,926 | T/G | — | uncertain significance |
| rs763042442 | 3:100,365,492 | G/A | — | uncertain significance |
| rs1056063815 | 3:100,365,500 | A/G | — | uncertain significance |
| rs763246023 | 3:100,365,534 | G/A | — | likely benign |
| rs770401736 | 3:100,365,552 | A/G | — | uncertain significance |
| rs964307769 | 3:100,368,566 | A/C | — | uncertain significance |
| rs781411508 | 3:100,368,588 | A/G | — | uncertain significance |
| rs368400475 | 3:100,368,596 | T/A | — | uncertain significance |
| rs2472337243 | 3:100,368,603 | T/C | — | uncertain significance |
| rs1289887177 | 3:100,368,620 | G/A | — | uncertain significance |
| rs7618197 | 3:100,370,773 | C/A | — | — |
| rs369701488 | 3:100,373,707 | G/A | — | uncertain significance |
| rs774350693 | 3:100,373,787 | G/T | — | uncertain significance |
| rs758734256 | 3:100,373,872 | A/G | — | uncertain significance |
| rs150034154 | 3:100,373,923 | A/C | — | uncertain significance |
| rs368926208 | 3:100,373,941 | G/A | — | uncertain significance |
| rs745983793 | 3:100,373,976 | G/A | — | uncertain significance |
| rs772948125 | 3:100,373,990 | G/A | — | likely benign |
| rs1167183646 | 3:100,374,015 | A/T | — | uncertain significance |
| rs41272977 | 3:100,374,810 | G/A | — | benign |
| rs756472958 | 3:100,374,826 | C/T | — | uncertain significance |
| rs150136013 | 3:100,378,576 | C/T | — | uncertain significance |
| rs374537120 | 3:100,378,585 | G/T | — | uncertain significance |
| rs1414252268 | 3:100,378,621 | G/A | — | uncertain significance |
| rs116022671 | 3:100,387,911 | G/T | — | uncertain significance |
| rs751160198 | 3:100,387,918 | G/A | — | uncertain significance |
| rs776502384 | 3:100,387,935 | T/C | — | uncertain significance |
| rs2472029866 | 3:100,413,615 | G/C | — | uncertain significance |
| rs780597144 | 3:100,413,630 | T/G | — | uncertain significance |
| rs115885846 | 3:100,413,642 | G/A | — | likely benign |
| rs145563365 | 3:100,413,683 | G/T | — | uncertain significance |
| rs762241234 | 3:100,413,709 | C/T | — | likely benign |
| rs9872512 | 3:100,413,718 | G/A | — | benign |
| rs2149046074 | 3:100,413,753 | A/G | — | likely benign |
| rs79517280 | 3:100,413,754 | C/A | — | conflicting classifications of pathogenicity |
| rs76785727 | 3:100,413,760 | A/G | — | conflicting classifications of pathogenicity |
| rs1019869787 | 3:100,413,766 | G/A | — | likely benign |
| rs765888895 | 3:100,413,790 | C/T | — | likely benign |
| rs753113675 | 3:100,413,808 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.