CSMD1

CUB and Sushi multiple domains 1

Summary

Predicted to act upstream of or within several processes, including learning or memory; mammary gland branching involved in pregnancy; and reproductive structure development. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants574 total

rsidPosition (GRCh37)AllelesClassClinVar
rs7577432718:2,796,114A/T—uncertain significance
rs3766758708:2,796,153G/C—uncertain significance
rs11653880028:2,796,195T/A—uncertain significance
rs13120387938:2,796,208C/T—uncertain significance
rs7512257428:2,796,221G/C—uncertain significance
rs7779235558:2,796,244T/C—uncertain significance
rs13839307288:2,796,261C/G—uncertain significance
rs5850008:2,796,277T/C—benign
rs7724440638:2,799,998G/T—uncertain significance
rs8892385558:2,800,087T/A—uncertain significance
rs119846918:2,800,096C/T—benign
rs7463030018:2,800,100A/T—uncertain significance
rs7699478648:2,800,107T/A—uncertain significance
rs3755245778:2,800,124G/C—benign
rs10195603338:2,800,130T/C—likely benign
rs7774590058:2,806,860G/T—uncertain significance
rs3684052038:2,806,865T/C—uncertain significance
rs13032345408:2,806,885T/C—likely benign
rs3728640088:2,806,892T/C—uncertain significance
rs24864862148:2,807,752C/T—uncertain significance
rs24864863958:2,807,773T/A—uncertain significance
rs24864869918:2,807,836G/C—uncertain significance
rs11879779978:2,807,863T/C—likely benign
rs2008252458:2,808,640C/T—likely benign
rs1858262178:2,808,648G/C—uncertain significance
rs7675352388:2,808,658C/T—likely benign
rs3753284798:2,808,667G/C—uncertain significance
rs343377128:2,808,730T/A—benign
rs7539439378:2,808,755T/A—uncertain significance
rs2020123128:2,808,777C/T—likely benign
rs3761605128:2,808,778G/A—likely benign
rs18026112078:2,808,800G/T—uncertain significance
rs1477681198:2,813,124C/T—benign
rs3774947248:2,813,180C/T—uncertain significance
rs7546689388:2,813,204T/A—uncertain significance
rs5666233718:2,813,255C/T—uncertain significance
rs7590347468:2,813,262C/T—likely benign
rs7587005138:2,815,256G/T—uncertain significance
rs18031227198:2,815,293A/G—uncertain significance
rs7751137668:2,815,309G/C—uncertain significance
rs10195009268:2,818,727T/C—uncertain significance
rs14614989148:2,818,736T/C—uncertain significance
rs48758578:2,819,809T/Cintron variant—
rs48758588:2,820,011C/T—uncertain significance
rs3738441448:2,820,024C/G—uncertain significance
rs7808914258:2,820,046G/A—likely benign
rs7689508458:2,820,054C/G—uncertain significance
rs1492249288:2,820,076C/T—benign
rs3683917228:2,820,077T/A—uncertain significance
rs1433710528:2,820,084A/C—likely benign
rs9502323408:2,820,098T/C—uncertain significance
rs3689684388:2,820,115A/G—likely benign
rs7725113028:2,820,122C/A—uncertain significance
rs7612475508:2,820,150C/T—uncertain significance
rs5418621948:2,820,751C/A—uncertain significance
rs24865979988:2,820,790G/T—likely benign
rs18036716088:2,820,887T/C—uncertain significance
rs355158478:2,820,895C/T—benign
rs7611153468:2,820,898C/T—likely benign
rs7651933218:2,820,912G/C—uncertain significance
rs7477166868:2,823,309G/T—uncertain significance
rs18039039448:2,823,312T/G—uncertain significance
rs1507133888:2,823,317G/A—uncertain significance
rs617440498:2,823,326C/G—likely benign
rs7565915078:2,823,333C/G—uncertain significance
rs24866193828:2,823,334T/G—uncertain significance
rs13041811208:2,823,336T/C—uncertain significance
rs1813327618:2,823,344C/A—uncertain significance
rs24866202998:2,823,396A/G—uncertain significance
rs7652535628:2,823,436G/C—uncertain significance
rs7773079018:2,823,443T/C—uncertain significance
rs7552769908:2,824,095T/G—uncertain significance
rs5278610398:2,824,101C/T—uncertain significance
rs7739148898:2,824,147C/G—uncertain significance
rs11771345808:2,824,238G/A—uncertain significance
rs1159912478:2,824,246G/C—benign
rs1176334528:2,824,257T/C—likely benign
rs24866862738:2,830,744T/A—uncertain significance
rs24866864378:2,830,755A/G—uncertain significance
rs18046195758:2,830,803C/A—uncertain significance
rs117849318:2,831,968C/T—benign
rs617431498:2,831,983G/C—benign
rs776976168:2,831,986C/A—benign
rs7687385238:2,832,030C/A—uncertain significance
rs1995719328:2,832,048C/T—uncertain significance
rs14168918398:2,832,051T/C—likely benign
rs1999973608:2,832,075C/T—benign
rs3688132218:2,832,105G/C—uncertain significance
rs7810527298:2,832,142T/C—uncertain significance
rs18047645738:2,832,146G/C—uncertain significance
rs2002021778:2,832,155A/G—likely benign
rs3687099618:2,836,125C/G—benign
rs12333333228:2,836,127G/A—uncertain significance
rs7815223948:2,836,176T/C—uncertain significance
rs1137934308:2,836,180G/C—benign
rs7675205338:2,836,257C/G—uncertain significance
rs3765698318:2,836,260G/A—uncertain significance
rs9410458158:2,836,263A/G—uncertain significance
rs2014573978:2,836,266T/A—uncertain significance
rs3720582058:2,836,268T/A—uncertain significance

Showing 100 of 574 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.