ABTB2

ankyrin repeat and BTB domain containing 2

Summary

Predicted to enable protein heterodimerization activity. Predicted to act upstream of or within cellular response to toxic substance. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants77 total

rsidPosition (GRCh37)AllelesClassClinVar
rs37277890611:34,173,951T/Clikely benign
rs128487536911:34,173,990G/Cuncertain significance
rs74616779311:34,174,029G/Auncertain significance
rs249625694211:34,174,043T/Guncertain significance
rs14102175311:34,174,046C/Tuncertain significance
rs15024877511:34,174,056C/Tuncertain significance
rs14630390511:34,174,096C/Guncertain significance
rs53928767611:34,175,835C/Tuncertain significance
rs144194524911:34,175,845C/Tuncertain significance
rs249625921411:34,175,865A/Guncertain significance
rs19992935011:34,180,875C/Tuncertain significance
rs142241596111:34,181,469C/Tuncertain significance
rs249626620211:34,181,514A/Guncertain significance
rs78065684011:34,181,806G/Auncertain significance
rs77065453211:34,181,818C/Tuncertain significance
rs55928233811:34,181,819G/Auncertain significance
rs249626705411:34,181,836G/Cuncertain significance
rs249626708711:34,181,848C/Guncertain significance
rs54040176211:34,181,891C/Tuncertain significance
rs11449980911:34,182,457G/Tuncertain significance
rs54475840311:34,182,461T/Guncertain significance
rs75145853011:34,182,599C/Tuncertain significance
rs91318833611:34,182,625A/Guncertain significance
rs75248525911:34,184,128G/Cuncertain significance
rs74722182111:34,184,153C/Tuncertain significance
rs20120939711:34,184,173T/Auncertain significance
rs77168281411:34,184,179A/Guncertain significance
rs75380080211:34,184,203C/Tuncertain significance
rs14232568211:34,184,222C/Guncertain significance
rs74544099411:34,184,231C/Tuncertain significance
rs93391783511:34,184,300G/Tuncertain significance
rs14354628711:34,184,308G/Auncertain significance
rs57697284511:34,184,348C/Tuncertain significance
rs123088047111:34,186,287G/Auncertain significance
rs75834074311:34,186,855C/Tuncertain significance
rs56239481411:34,186,872C/Tuncertain significance
rs76255145911:34,188,871G/Auncertain significance
rs36952210711:34,188,877T/Clikely benign
rs249627754011:34,188,904G/Auncertain significance
rs13997370611:34,189,512C/Tuncertain significance
rs75169797611:34,189,530G/Tuncertain significance
rs74798066311:34,192,459A/Cuncertain significance
rs53371333711:34,192,554G/Cuncertain significance
rs249628203611:34,192,588C/Auncertain significance
rs76892466711:34,192,593G/Auncertain significance
rs249628577511:34,194,705A/Guncertain significance
rs76338734311:34,194,711C/Tuncertain significance
rs14226549511:34,194,775C/Tuncertain significance
rs97726912611:34,194,784T/Cuncertain significance
rs75716357611:34,194,786C/Tuncertain significance
rs185291108811:34,194,807A/Guncertain significance
rs76940160311:34,218,900G/Tuncertain significance
rs249440232811:34,218,912G/Auncertain significance
rs249440239711:34,218,938C/Tuncertain significance
rs77367852411:34,218,950T/Auncertain significance
rs185327209311:34,218,951A/Cuncertain significance
rs75056740111:34,219,001T/Cuncertain significance
rs56082578111:34,219,013C/Tuncertain significance
rs74763196711:34,219,014G/Auncertain significance
rs77334992611:34,219,047G/Auncertain significance
rs133769440011:34,226,220C/Guncertain significance
rs1280497511:34,246,114G/T
rs18459654811:34,288,716G/Aintron variant
rs14809700111:34,298,445G/Aintron variant
rs77389992111:34,378,362C/Tuncertain significance
rs75633378811:34,378,428T/Cuncertain significance
rs125518241311:34,378,481G/Auncertain significance
rs117689006811:34,378,496C/Auncertain significance
rs140003370211:34,378,604A/Tuncertain significance
rs76287349211:34,378,638C/Guncertain significance
rs76636172611:34,378,661T/Cuncertain significance
rs95155946711:34,378,737G/Auncertain significance
rs213313348211:34,378,802T/Cuncertain significance
rs249455264611:34,378,891T/Auncertain significance
rs145947677111:34,378,941G/Auncertain significance
rs55534584711:34,379,048C/Guncertain significance
rs249455306511:34,379,060C/Tuncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.