ADGRA2
adhesion G protein-coupled receptor A2
Summary
Predicted to enable G protein-coupled receptor activity. Involved in canonical Wnt signaling pathway. Located in intracellular membrane-bounded organelle and plasma membrane. Part of Wnt signalosome. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants96 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2487431742 | 8:37,654,826 | C/A | — | uncertain significance |
| rs1804359522 | 8:37,654,874 | G/A | — | uncertain significance |
| rs1176916512 | 8:37,654,886 | G/T | — | likely benign |
| rs1211538147 | 8:37,654,955 | G/C | — | uncertain significance |
| rs767208463 | 8:37,654,964 | G/A | — | uncertain significance |
| rs774253377 | 8:37,655,030 | C/A | — | uncertain significance |
| rs2487472322 | 8:37,672,436 | A/G | — | uncertain significance |
| rs267601911 | 8:37,672,445 | C/T | — | uncertain significance |
| rs1487221783 | 8:37,672,451 | G/A | — | uncertain significance |
| rs12676965 | 8:37,681,426 | T/C | intron variant | — |
| rs555460019 | 8:37,681,699 | G/A | — | — |
| rs1466215650 | 8:37,686,414 | G/C | — | uncertain significance |
| rs6468442 | 8:37,686,749 | A/G | regulatory region variant | — |
| rs769862036 | 8:37,686,795 | C/T | — | uncertain significance |
| rs150153046 | 8:37,686,816 | G/A | — | uncertain significance |
| rs1335119235 | 8:37,686,837 | A/G | — | uncertain significance |
| rs145560238 | 8:37,686,847 | G/A | — | uncertain significance |
| rs1805403031 | 8:37,687,392 | C/T | — | uncertain significance |
| rs368184891 | 8:37,687,470 | C/T | — | uncertain significance |
| rs769727910 | 8:37,687,516 | G/T | — | uncertain significance |
| rs771754787 | 8:37,688,264 | C/A | — | uncertain significance |
| rs777238816 | 8:37,688,293 | G/A | — | uncertain significance |
| rs2487518729 | 8:37,688,350 | T/C | — | uncertain significance |
| rs1805432547 | 8:37,688,352 | G/T | — | uncertain significance |
| rs1046858116 | 8:37,688,387 | A/G | — | uncertain significance |
| rs201617128 | 8:37,688,390 | C/G | — | uncertain significance |
| rs111714720 | 8:37,688,966 | G/A | — | uncertain significance |
| rs779364501 | 8:37,689,017 | G/A | — | uncertain significance |
| rs376961808 | 8:37,690,611 | C/A | — | uncertain significance |
| rs772813438 | 8:37,690,613 | C/T | — | uncertain significance |
| rs753302682 | 8:37,690,623 | G/A | — | uncertain significance |
| rs764578995 | 8:37,690,632 | G/A | — | uncertain significance |
| rs200841231 | 8:37,690,634 | C/T | — | uncertain significance |
| rs1357273209 | 8:37,690,652 | C/T | — | uncertain significance |
| rs200541731 | 8:37,690,653 | G/A | — | uncertain significance |
| rs770139947 | 8:37,691,258 | A/T | — | uncertain significance |
| rs369743546 | 8:37,691,558 | G/A | — | uncertain significance |
| rs201472750 | 8:37,691,579 | G/A | — | uncertain significance |
| rs758837731 | 8:37,691,584 | G/A | — | uncertain significance |
| rs143101001 | 8:37,691,603 | T/C | — | uncertain significance |
| rs763526015 | 8:37,691,645 | T/G | — | uncertain significance |
| rs115247446 | 8:37,691,651 | T/C | — | benign |
| rs147459946 | 8:37,692,696 | C/T | — | uncertain significance |
| rs2487532090 | 8:37,692,723 | T/A | — | uncertain significance |
| rs532029404 | 8:37,692,789 | C/T | — | uncertain significance |
| rs148475803 | 8:37,692,825 | C/T | — | uncertain significance |
| rs776152455 | 8:37,692,830 | G/A | — | uncertain significance |
| rs1405023262 | 8:37,692,860 | C/T | — | uncertain significance |
| rs754039771 | 8:37,692,878 | G/A | — | uncertain significance |
| rs146483342 | 8:37,692,882 | G/A | — | uncertain significance |
| rs760530594 | 8:37,693,118 | C/T | — | uncertain significance |
| rs763915452 | 8:37,693,192 | C/T | — | uncertain significance |
| rs368535918 | 8:37,693,222 | C/T | — | uncertain significance |
| rs778110980 | 8:37,693,250 | G/A | — | uncertain significance |
| rs146016051 | 8:37,693,251 | G/A | — | benign |
| rs77369926 | 8:37,693,279 | G/A | — | benign |
| rs2487541864 | 8:37,695,264 | G/A | — | uncertain significance |
| rs768890920 | 8:37,695,296 | C/T | — | uncertain significance |
| rs375163748 | 8:37,695,302 | T/C | — | uncertain significance |
| rs200831475 | 8:37,695,317 | G/A | — | uncertain significance |
| rs1044641803 | 8:37,695,363 | G/A | — | uncertain significance |
| rs760136473 | 8:37,695,375 | C/T | — | uncertain significance |
| rs901613763 | 8:37,695,452 | C/T | — | uncertain significance |
| rs143113584 | 8:37,696,483 | G/A | — | uncertain significance |
| rs758313655 | 8:37,696,544 | C/T | — | uncertain significance |
| rs1805728412 | 8:37,697,080 | G/A | — | uncertain significance |
| rs139902661 | 8:37,697,124 | A/G | — | uncertain significance |
| rs767967328 | 8:37,697,697 | C/T | — | uncertain significance |
| rs1443346346 | 8:37,697,730 | C/T | — | uncertain significance |
| rs148423972 | 8:37,697,735 | C/A | — | uncertain significance |
| rs757191897 | 8:37,697,783 | C/T | — | uncertain significance |
| rs142650653 | 8:37,698,291 | G/T | — | uncertain significance |
| rs757131775 | 8:37,698,363 | C/G | — | uncertain significance |
| rs2487553745 | 8:37,698,614 | G/A | — | uncertain significance |
| rs142683741 | 8:37,698,852 | G/A | — | uncertain significance |
| rs1225288397 | 8:37,698,884 | G/A | — | uncertain significance |
| rs761350049 | 8:37,698,900 | C/T | — | uncertain significance |
| rs113275053 | 8:37,698,902 | G/C | — | benign |
| rs568141708 | 8:37,698,927 | C/G | — | uncertain significance |
| rs139962707 | 8:37,698,983 | C/T | — | uncertain significance |
| rs868836566 | 8:37,699,100 | G/T | — | uncertain significance |
| rs760019897 | 8:37,699,136 | G/T | — | uncertain significance |
| rs746003915 | 8:37,699,179 | C/T | — | uncertain significance |
| rs1003522135 | 8:37,699,223 | G/C | — | uncertain significance |
| rs111828443 | 8:37,699,293 | T/C | — | benign |
| rs1257884306 | 8:37,699,341 | C/G | — | uncertain significance |
| rs762298535 | 8:37,699,431 | C/A | — | uncertain significance |
| rs1402005064 | 8:37,699,481 | G/A | — | uncertain significance |
| rs1805818517 | 8:37,699,587 | T/C | — | uncertain significance |
| rs1054795133 | 8:37,699,649 | G/A | — | uncertain significance |
| rs1438288788 | 8:37,699,653 | C/T | — | uncertain significance |
| rs746259780 | 8:37,699,682 | A/G | — | uncertain significance |
| rs546264591 | 8:37,699,704 | G/C | — | uncertain significance |
| rs2487560498 | 8:37,699,713 | T/C | — | uncertain significance |
| rs1805827468 | 8:37,699,769 | G/A | — | uncertain significance |
| rs757967284 | 8:37,699,845 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.