XRCC2

X-ray repair cross complementing 2

Summary

This gene encodes a member of the RecA/Rad51-related protein family that participates in homologous recombination to maintain chromosome stability and repair DNA damage. This gene is involved in the repair of DNA double-strand breaks by homologous recombination and it functionally complements Chinese hamster irs1, a repair-deficient mutant that exhibits hypersensitivity to a number of different DNA-damaging agents. [provided by RefSeq, Jul 2008]

Known Variants495 total

rsidPosition (GRCh37)AllelesClassClinVar
rs32185537:152,343,802T/G—uncertain significance
rs32185417:152,345,544G/A—benign
rs32185407:152,345,687C/G—benign
rs32185397:152,345,726A/G—benign
rs7575103597:152,345,728C/T—likely benign
rs12686835057:152,345,730A/G—likely benign
rs20980270747:152,345,731C/T—uncertain significance
rs24858801117:152,345,736T/C—likely benign
rs24858801137:152,345,737T/C—uncertain significance
rs21169868677:152,345,738C/T—uncertain significance
rs7458771637:152,345,741C/A—uncertain significance
rs15901291467:152,345,742C/T—conflicting classifications of pathogenicity
rs21169868817:152,345,743C/T—uncertain significance
rs7308820447:152,345,744C/T—uncertain significance
rs7704386507:152,345,745A/C—uncertain significance
rs7496843717:152,345,748T/G—uncertain significance
rs10647940617:152,345,749T/C—uncertain significance
rs21169869337:152,345,752C/T—uncertain significance
rs12923173537:152,345,753C/T—uncertain significance
rs5877801327:152,345,759T/C—uncertain significance
rs24858801867:152,345,761A/C—uncertain significance
rs1450857427:152,345,762A/C—likely benign
rs24858801957:152,345,763A/C—uncertain significance
rs7614764737:152,345,765A/G—uncertain significance
rs24858802037:152,345,766A/T—uncertain significance
rs24858802127:152,345,768G/A—uncertain significance
rs14338534297:152,345,769T/G—uncertain significance
rs11592350247:152,345,775T/A—uncertain significance
rs7716719717:152,345,776A/G—uncertain significance
rs11923914167:152,345,777A/T—uncertain significance
rs20980271157:152,345,778A/G—likely benign
rs24858802387:152,345,779C/T—likely benign
rs13951301437:152,345,781G/C—uncertain significance
rs24858802777:152,345,786T/C—uncertain significance
rs14231936077:152,345,787T/G—uncertain significance
rs1504746767:152,345,788T/G—uncertain significance
rs1383349327:152,345,793A/G—likely benign
rs21169870287:152,345,794C/T—uncertain significance
rs1491869337:152,345,797C/T—conflicting classifications of pathogenicity
rs7593002527:152,345,798G/A—uncertain significance
rs7308820477:152,345,800G/A—uncertain significance
rs24858803137:152,345,811A/T—uncertain significance
rs15901292177:152,345,814T/C—likely benign
rs15901292217:152,345,816G/C—uncertain significance
rs7525034257:152,345,817G/C—conflicting classifications of pathogenicity
rs11713543437:152,345,820G/A—likely benign
rs20980271407:152,345,821C/G—uncertain significance
rs7815074997:152,345,824C/G—uncertain significance
rs1138113097:152,345,827T/G—likely benign
rs1909005607:152,345,828G/C—conflicting classifications of pathogenicity
rs7804637687:152,345,830G/A—uncertain significance
rs24858803627:152,345,831A/G—uncertain significance
rs7497791417:152,345,836T/C—uncertain significance
rs9144645017:152,345,837C/A—uncertain significance
rs15901292467:152,345,839T/C—uncertain significance
rs10647959547:152,345,840G/A—uncertain significance
rs15901292517:152,345,842T/G—uncertain significance
rs24858803917:152,345,843T/C—uncertain significance
rs21169871147:152,345,844G/A—likely benign
rs20980271577:152,345,845G/A—uncertain significance
rs7689947847:152,345,847G/A—likely benign
rs24858804077:152,345,849A/C—uncertain significance
rs10575217537:152,345,850A/G—likely benign
rs24858804117:152,345,852A/C—uncertain significance
rs24858804167:152,345,853C/T—likely benign
rs5347463307:152,345,856C/G—uncertain significance
rs10647941627:152,345,857C/T—uncertain significance
rs7533682677:152,345,859G/A—likely benign
rs21169871407:152,345,860T/A—uncertain significance
rs15901292767:152,345,867C/G—uncertain significance
rs21169871637:152,345,868C/T—likely benign
rs24858804577:152,345,869A/G—uncertain significance
rs32185387:152,345,871T/C—likely benign
rs9460753167:152,345,872T/A—uncertain significance
rs21169871847:152,345,876G/A—uncertain significance
rs12674629137:152,345,877C/A—uncertain significance
rs24858805507:152,345,879A/G—uncertain significance
rs21169871967:152,345,880T/C—likely benign
rs24858805537:152,345,881G/A—uncertain significance
rs20980271737:152,345,883C/G—uncertain significance
rs24858805597:152,345,885T/C—uncertain significance
rs7717227507:152,345,888A/G—uncertain significance
rs20980271777:152,345,889G/A—likely benign
rs13844176287:152,345,891G/C—uncertain significance
rs1433576177:152,345,892A/C—uncertain significance
rs24858805867:152,345,893T/A—uncertain significance
rs24858805917:152,345,895A/C—likely benign
rs24858805977:152,345,896G/A—uncertain significance
rs9233971127:152,345,897G/A—uncertain significance
rs24858806037:152,345,898T/G—uncertain significance
rs13333766117:152,345,899C/G—uncertain significance
rs3742130937:152,345,901G/A—likely benign
rs24858806177:152,345,902T/C—uncertain significance
rs5877801307:152,345,903A/G—uncertain significance
rs24858806307:152,345,906C/A—uncertain significance
rs32185377:152,345,908A/G—conflicting classifications of pathogenicity
rs9326411967:152,345,909T/C—likely benign
rs13791194327:152,345,910G/A—likely benign
rs7650217417:152,345,911T/A—uncertain significance
rs13564982037:152,345,912C/T—uncertain significance

Showing 100 of 495 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.