ODAD1

outer dynein arm docking complex subunit 1

Summary

This gene encodes a coiled-coil domain-containing protein that is a component of the outer dynein arm docking complex in cilia cells. Mutations in this gene may cause primary ciliary dyskinesia 20. [provided by RefSeq, May 2013]

Known Variants393 total

rsidPosition (GRCh37)AllelesClassClinVar
rs1041364019:48,799,991C/T—benign
rs1041582519:48,800,218C/T—benign
rs116164136719:48,800,236G/T—likely benign
rs53931480719:48,800,240C/T—likely benign
rs20036969319:48,800,241G/A—uncertain significance
rs251592331919:48,800,252C/G—uncertain significance
rs57258987019:48,800,266C/T—likely benign
rs76859860919:48,800,267G/A—uncertain significance
rs87885521019:48,800,287G/A—likely benign
rs75036310219:48,800,290G/A—likely benign
rs14412877319:48,800,301C/T—conflicting classifications of pathogenicity
rs75422149219:48,800,310T/C—uncertain significance
rs251592352819:48,800,313T/C—uncertain significance
rs251592354619:48,800,317C/T—likely benign
rs75762636519:48,800,319C/T—uncertain significance
rs77929776619:48,800,320G/A—likely benign
rs77173479219:48,800,328C/T—uncertain significance
rs14652188019:48,800,329G/T—uncertain significance
rs7435163519:48,800,330T/C—benign
rs146512366419:48,800,332C/G—likely benign
rs7492505619:48,800,333A/G—benign
rs725298819:48,800,338G/A—benign
rs76283806519:48,800,341C/T—likely benign
rs14018911419:48,800,352C/T—uncertain significance
rs18101126019:48,800,353G/A—likely benign
rs75092020619:48,800,363C/G—uncertain significance
rs160085444419:48,800,368C/A—uncertain significance
rs92962598519:48,800,382C/T—uncertain significance
rs15033519419:48,800,383G/A—likely benign
rs138042412019:48,800,384C/T—uncertain significance
rs196830999019:48,800,387C/T—uncertain significance
rs78067960119:48,800,400C/T—uncertain significance
rs78072322419:48,800,420T/A—uncertain significance
rs13919395419:48,800,423C/G—uncertain significance
rs77310828919:48,800,425G/C—uncertain significance
rs20157196319:48,800,430C/A—likely benign
rs54803510819:48,800,431G/A—likely benign
rs251592406519:48,800,432C/T—uncertain significance
rs77425731019:48,800,436C/T—uncertain significance
rs75086152719:48,800,451C/T—uncertain significance
rs75883294919:48,800,452G/A—likely benign
rs14321961819:48,800,465G/A—uncertain significance
rs14752701419:48,800,468G/A—uncertain significance
rs196831453019:48,800,477G/A—uncertain significance
rs56332117019:48,800,481C/T—uncertain significance
rs77065380019:48,800,482G/A—likely benign
rs13856240119:48,800,491G/A—likely benign
rs55062000619:48,800,513T/C—uncertain significance
rs36856028419:48,800,515C/T—likely benign
rs37288907719:48,800,516G/A—uncertain significance
rs20197830519:48,800,535G/A—uncertain significance
rs75341909519:48,800,556C/T—uncertain significance
rs57042520119:48,800,557G/A—likely benign
rs20012433519:48,800,558C/G—uncertain significance
rs14422523019:48,800,561A/G—uncertain significance
rs14707202619:48,800,569G/A—likely benign
rs77985469219:48,800,571G/A—uncertain significance
rs251592451619:48,800,574C/G—uncertain significance
rs55930221219:48,800,585C/T—uncertain significance
rs36982583519:48,800,586G/A—uncertain significance
rs14230143719:48,800,619C/T—uncertain significance
rs1334632319:48,800,620G/A—benign
rs139447846619:48,800,623G/A—likely benign
rs133547874619:48,800,630T/C—uncertain significance
rs196832330519:48,800,649C/T—uncertain significance
rs19096499619:48,800,655C/G—uncertain significance
rs90887752519:48,800,656G/A—likely benign
rs144981780719:48,800,667C/T—likely benign
rs13927093219:48,800,668G/A—likely benign
rs13826203119:48,800,677G/T—likely benign
rs251592478519:48,800,683G/A—likely benign
rs120681136019:48,800,684G/A—uncertain significance
rs11512460419:48,800,685C/T—likely benign
rs77134617719:48,800,695G/A—likely benign
rs77470200619:48,800,696C/G—uncertain significance
rs7472245119:48,800,707G/A—likely benign
rs77609346719:48,800,709C/A—uncertain significance
rs86711310719:48,800,711A/G—uncertain significance
rs37416033219:48,800,716C/T—likely benign
rs77615616119:48,800,717G/A—uncertain significance
rs76493210319:48,800,719G/A—likely benign
rs11411102019:48,800,721C/T—likely benign
rs75822110119:48,800,722G/A—likely benign
rs7358533219:48,800,725G/A—benign
rs7441300519:48,800,727C/T—likely benign
rs75501443219:48,800,728G/A—likely benign
rs251592500619:48,800,729G/A—uncertain significance
rs78124457219:48,800,733G/A—likely benign
rs74943583119:48,800,744C/T—likely benign
rs20059831219:48,800,745G/A—uncertain significance
rs20002279919:48,800,749C/T—likely benign
rs6174775419:48,800,751C/A—benign
rs74736333419:48,800,755C/T—likely benign
rs76132829619:48,800,757C/T—uncertain significance
rs229211319:48,800,791A/G—benign
rs141869077819:48,800,827C/G—likely benign
rs18275062619:48,800,830G/A—benign
rs77399686719:48,800,842C/T—uncertain significance
rs75940947019:48,800,843T/C—uncertain significance
rs37185456919:48,800,849G/T—uncertain significance

Showing 100 of 393 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.