CSMD3

CUB and Sushi multiple domains 3

Summary

Predicted to be involved in regulation of dendrite development. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants239 total

rsidPosition (GRCh37)AllelesClassClinVar
rs48764588:113,237,045T/C—benign
rs7475342568:113,237,097G/A—uncertain significance
rs1383216728:113,241,021A/G—uncertain significance
rs3704452338:113,241,052T/G—uncertain significance
rs7566324038:113,241,066C/T—uncertain significance
rs15926248:113,241,088G/T—benign
rs21298918438:113,243,788C/T—uncertain significance
rs3684789538:113,246,587T/C—likely benign
rs1151353958:113,246,660A/G—benign
rs7547531898:113,246,670C/T—likely benign
rs12060060228:113,249,436A/C—uncertain significance
rs25374251338:113,249,437T/C—uncertain significance
rs7505338868:113,249,458C/T—uncertain significance
rs7744199338:113,249,526A/G—uncertain significance
rs617537368:113,253,954G/A—benign
rs18144960018:113,256,662A/C—uncertain significance
rs18145021578:113,256,704C/G—uncertain significance
rs2019967938:113,256,748T/A—uncertain significance
rs21301146758:113,256,778G/A—uncertain significance
rs7688778228:113,256,786C/G—uncertain significance
rs1420184788:113,259,328T/C—likely benign
rs18148118118:113,259,354T/C—uncertain significance
rs3771978838:113,259,364T/C—likely benign
rs1435722528:113,266,491G/A—benign
rs7601912868:113,266,499T/C—uncertain significance
rs7762521118:113,266,504T/G—uncertain significance
rs10363670998:113,267,545C/T—uncertain significance
rs15636945868:113,267,576A/G—uncertain significance
rs105051828:113,268,098G/Tintron variant—
rs168833238:113,275,878C/T—benign
rs13336521608:113,275,888C/T—uncertain significance
rs3705299228:113,275,982C/T—uncertain significance
rs1152087688:113,275,998C/A—benign
rs14346883088:113,276,021G/A—uncertain significance
rs617537388:113,276,045C/A—benign
rs1448999388:113,277,717G/A—uncertain significance
rs7560914908:113,277,741G/A—uncertain significance
rs7737526918:113,277,774T/C—uncertain significance
rs7626595718:113,277,814T/A—uncertain significance
rs7575484808:113,293,543C/T—uncertain significance
rs15866581288:113,299,284T/G—likely benign
rs1874830498:113,299,350C/T—uncertain significance
rs1450270718:113,299,353A/G—benign
rs5505950108:113,299,415C/T—uncertain significance
rs1439255138:113,301,634T/C—likely benign
rs5667020498:113,301,663G/A—uncertain significance
rs1996041708:113,301,668C/T—uncertain significance
rs21934308:113,301,744C/G—benign
rs18195511738:113,301,766C/T—uncertain significance
rs1149265228:113,303,848G/A—likely benign
rs3729983518:113,304,761T/C—likely benign
rs21306882748:113,304,801T/G—uncertain significance
rs1399683078:113,304,809G/A—likely benign
rs21306893148:113,304,847T/C—uncertain significance
rs5550619088:113,304,883A/C—uncertain significance
rs2021778708:113,304,947G/A—likely benign
rs617545298:113,308,072T/A—benign
rs7663871748:113,308,074G/A—uncertain significance
rs7669026598:113,308,090A/T—uncertain significance
rs2006183978:113,308,175C/T—uncertain significance
rs3771842488:113,308,178T/C—uncertain significance
rs5648777178:113,308,232C/T—uncertain significance
rs48764628:113,308,243A/G—benign
rs10377665028:113,314,031T/C—uncertain significance
rs7725747588:113,314,111G/C—uncertain significance
rs25379164068:113,314,123G/A—uncertain significance
rs7641463008:113,314,134T/C—likely benign
rs1500850798:113,314,149A/G—likely benign
rs7795388428:113,314,180T/A—uncertain significance
rs7684404908:113,316,962G/T—uncertain significance
rs340701278:113,317,026A/C—benign
rs21307785838:113,317,061T/C—uncertain significance
rs21307870698:113,318,305C/G—uncertain significance
rs3717712488:113,318,343G/T—uncertain significance
rs5611779088:113,318,367T/C—uncertain significance
rs21308128328:113,323,233C/A—uncertain significance
rs3748831468:113,323,331C/A—uncertain significance
rs1418645458:113,323,338C/T—uncertain significance
rs18222308108:113,326,197A/G—uncertain significance
rs21308319368:113,326,249G/A—uncertain significance
rs14725396608:113,326,254A/G—uncertain significance
rs1393339088:113,326,269T/C—likely benign
rs2017038808:113,326,651T/C—likely benign
rs7547109888:113,326,695C/G—uncertain significance
rs1499301408:113,326,701G/T—uncertain significance
rs1486402808:113,326,822C/T—uncertain significance
rs1999989528:113,326,823G/A—uncertain significance
rs1420900418:113,331,092A/G—uncertain significance
rs3687211898:113,331,098A/C—uncertain significance
rs2005154248:113,331,101C/T—uncertain significance
rs1456998398:113,332,187G/A—likely benign
rs21308674848:113,332,203T/A—uncertain significance
rs21309465128:113,347,553C/T—uncertain significance
rs617545288:113,347,559G/A—likely benign
rs3722569888:113,347,625T/C—likely benign
rs1134497038:113,347,652G/A—likely benign
rs10392068138:113,347,672C/T—uncertain significance
rs1832433588:113,348,942C/T—uncertain significance
rs12582184558:113,348,954G/A—uncertain significance
rs21309589088:113,349,039T/C—uncertain significance

Showing 100 of 239 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.