ADGRG3

adhesion G protein-coupled receptor G3

Summary

Predicted to enable G protein-coupled receptor activity. Involved in G protein-coupled receptor signaling pathway and regulation of cell migration. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants42 total

rsidPosition (GRCh37)AllelesClassClinVar
rs76002947416:57,702,309C/Tlikely benign
rs75382944516:57,707,286A/Tuncertain significance
rs36801730516:57,707,292G/Auncertain significance
rs14411712416:57,707,311A/Guncertain significance
rs146153222416:57,707,312C/Guncertain significance
rs13998412416:57,707,328A/Guncertain significance
rs77035896616:57,707,335G/Tuncertain significance
rs77595476916:57,707,337A/Guncertain significance
rs76510704716:57,707,352G/Alikely benign
rs77810052316:57,710,195A/Guncertain significance
rs76248081016:57,710,219A/Guncertain significance
rs14256149616:57,712,086C/Tuncertain significance
rs74760935016:57,712,106G/Auncertain significance
rs37550025416:57,712,142A/Tuncertain significance
rs75776379716:57,712,160C/Tuncertain significance
rs14069200416:57,712,182G/Auncertain significance
rs14794734716:57,713,096G/Alikely benign
rs77210149116:57,713,102G/Tuncertain significance
rs76151688416:57,713,119G/Alikely benign
rs37615443716:57,713,122G/Auncertain significance
rs14920175716:57,713,135G/Alikely benign
rs20133404516:57,713,150G/Auncertain significance
rs96038111916:57,714,179A/Clikely benign
rs37334562916:57,714,213C/Auncertain significance
rs75387402416:57,714,233A/Tuncertain significance
rs77798653016:57,714,266G/Auncertain significance
rs19995613416:57,714,269C/Auncertain significance
rs75460666316:57,714,480G/Auncertain significance
rs250658688516:57,714,487T/Cuncertain significance
rs250660852216:57,717,954C/Tuncertain significance
rs86647776616:57,717,983C/Tuncertain significance
rs14864414916:57,717,984G/Cuncertain significance
rs14565107816:57,718,115G/Auncertain significance
rs20190015816:57,719,601G/Auncertain significance
rs250662166716:57,719,610T/Cuncertain significance
rs102003968516:57,719,659T/Clikely benign
rs15074172916:57,719,704G/Alikely benign
rs20013070216:57,719,746C/Tuncertain significance
rs56362724116:57,719,805G/Alikely benign
rs76467769416:57,722,305A/Guncertain significance
rs14799443116:57,722,358C/Tlikely benign
rs77358080916:57,722,359G/Auncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.