ADGRA3

adhesion G protein-coupled receptor A3

Summary

This gene encodes a member of the G protein-coupled receptor superfamily. This membrane protein may play a role in tumor angiogenesis through its interaction with the human homolog of the Drosophila disc large tumor suppressor gene. This gene is mapped to a candidate region of chromosome 4 which may be associated with bipolar disorder and schizophrenia. [provided by RefSeq, Oct 2012]

Known Variants810 total

rsidPosition (GRCh37)AllelesClassClinVar
rs24746850854:22,389,335G/A—uncertain significance
rs7515316704:22,389,343G/C—uncertain significance
rs5438885464:22,389,362C/T—uncertain significance
rs1449076604:22,389,368T/C—uncertain significance
rs24746851594:22,389,371C/A—uncertain significance
rs13512075394:22,389,375T/G—uncertain significance
rs5558073394:22,389,376G/Asynonymous variant—
rs5683181704:22,389,378T/A—uncertain significance
rs9288535084:22,389,381C/T—uncertain significance
rs7564090204:22,389,382G/A—likely benign
rs1477162234:22,389,387C/A—uncertain significance
rs13511100914:22,389,401T/G—uncertain significance
rs17139016824:22,389,409A/T—uncertain significance
rs24746853164:22,389,417T/C—uncertain significance
rs7764040754:22,389,419A/G—uncertain significance
rs14407177944:22,389,423G/A—uncertain significance
rs7651473814:22,389,428T/C—uncertain significance
rs24746853624:22,389,432G/A—uncertain significance
rs7517220494:22,389,442G/A—likely benign
rs8979224444:22,389,447G/A—uncertain significance
rs1492997524:22,389,449C/G—uncertain significance
rs7682694844:22,389,451A/G—likely benign
rs1445689774:22,389,456A/G—uncertain significance
rs12748573914:22,389,457T/G—uncertain significance
rs1426531464:22,389,464T/C—uncertain significance
rs21089880444:22,389,467T/C—uncertain significance
rs1468971254:22,389,468T/G—conflicting classifications of pathogenicity
rs1471623044:22,389,480C/T—uncertain significance
rs1142322884:22,389,484A/T—benign
rs5641042044:22,389,500G/A—uncertain significance
rs7628307014:22,389,501C/T—uncertain significance
rs1441720184:22,389,503T/C—uncertain significance
rs17139086764:22,389,507T/G—uncertain significance
rs7620440744:22,389,513T/C—uncertain significance
rs24746855924:22,389,517G/C—likely benign
rs21089881194:22,389,524A/G—uncertain significance
rs13978577484:22,389,527G/A—uncertain significance
rs17139111374:22,389,555G/A—uncertain significance
rs11697374144:22,389,562G/C—uncertain significance
rs7553035184:22,389,566C/T—uncertain significance
rs7655338794:22,389,567A/G—uncertain significance
rs7568955564:22,389,573C/T—uncertain significance
rs9775584584:22,389,580G/A—likely benign
rs1511170154:22,389,582C/T—uncertain significance
rs1400318244:22,389,596T/C—uncertain significance
rs7491413414:22,389,603G/C—uncertain significance
rs1448957494:22,389,607C/T—likely benign
rs11958928004:22,389,615A/G—uncertain significance
rs7607375074:22,389,630T/C—uncertain significance
rs1406560464:22,389,632C/T—benign
rs7599894054:22,389,641G/A—uncertain significance
rs17139171854:22,389,650T/C—uncertain significance
rs8679564564:22,389,652G/A—likely benign
rs1443145354:22,389,653T/G—uncertain significance
rs14724947744:22,389,656T/C—uncertain significance
rs7568766064:22,389,662A/G—uncertain significance
rs7671906704:22,389,664C/T—likely benign
rs3679463714:22,389,665C/T—uncertain significance
rs7796592764:22,389,666G/A—uncertain significance
rs21089883484:22,389,671T/C—uncertain significance
rs17139192114:22,389,679G/A—likely benign
rs17139193414:22,389,681C/T—uncertain significance
rs1465694964:22,389,682G/A—conflicting classifications of pathogenicity
rs24746860324:22,389,684T/C—uncertain significance
rs1412227764:22,389,690C/T—uncertain significance
rs7722505864:22,389,691G/A—likely benign
rs7471397964:22,389,702C/T—uncertain significance
rs7710236894:22,389,703G/A—likely benign
rs13533054784:22,389,704C/T—uncertain significance
rs617293614:22,389,707G/A—uncertain significance
rs7633758164:22,389,708T/C—uncertain significance
rs12551677354:22,389,712G/C—likely benign
rs17139226044:22,389,714C/T—uncertain significance
rs7671198644:22,389,718G/A—likely benign
rs10079923554:22,389,724A/G—likely benign
rs21089884764:22,389,725T/C—uncertain significance
rs15602905374:22,389,736G/T—likely benign
rs3708611364:22,389,749C/T—uncertain significance
rs15773159114:22,389,751T/G—likely benign
rs7659903404:22,389,755C/T—uncertain significance
rs7533385614:22,389,756G/A—uncertain significance
rs3707675674:22,389,785C/T—uncertain significance
rs7581888464:22,389,786G/A—uncertain significance
rs3735315434:22,389,788C/T—uncertain significance
rs21089885884:22,389,794T/G—uncertain significance
rs38144164:22,389,797A/C—benign
rs17139274344:22,389,798C/T—uncertain significance
rs24746863454:22,389,799A/G—likely benign
rs17139275334:22,389,800T/G—uncertain significance
rs7710769734:22,389,806C/T—uncertain significance
rs7767059894:22,389,811C/A—uncertain significance
rs24746863794:22,389,813G/T—uncertain significance
rs1892923824:22,389,814A/G—likely benign
rs1996169444:22,389,816C/T—uncertain significance
rs24746864044:22,389,823A/G—likely benign
rs1482268404:22,389,826C/T—benign
rs7760383804:22,389,827G/A—uncertain significance
rs7632793774:22,389,831C/T—uncertain significance
rs5741520514:22,389,832G/A—likely benign
rs7747859294:22,389,835C/T—uncertain significance

Showing 100 of 810 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.