GOSR2

golgi SNAP receptor complex member 2

Summary

This gene encodes a trafficking membrane protein which transports proteins among the medial- and trans-Golgi compartments. Due to its chromosomal location and trafficking function, this gene may be involved in familial essential hypertension. [provided by RefSeq, Mar 2016]

Known Variants281 total

rsidPosition (GRCh37)AllelesClassClinVar
rs5590408517:45,000,234C/T—benign
rs7637447817:45,000,354C/T—benign
rs88605307617:45,000,495G/T—uncertain significance
rs105752340317:45,000,525C/T—likely benign
rs18989917:45,000,529G/C—benign
rs76991876317:45,000,530C/T—likely benign
rs36989288517:45,000,533G/C—benign
rs56223702117:45,000,536C/A—benign
rs76852639717:45,000,537C/G—likely benign
rs88605307717:45,000,539T/G—uncertain significance
rs37319279117:45,000,543C/G—benign
rs18319917:45,000,547G/C—benign
rs76001820017:45,000,552C/G—uncertain significance
rs57404574617:45,000,558C/T—uncertain significance
rs87932885517:45,000,559A/C—likely pathogenic
rs75171218117:45,000,560T/G—pathogenic
rs117410426017:45,000,561G/A—uncertain significance
rs142544209817:45,000,562G/A—uncertain significance
rs141349648417:45,000,563A/C—uncertain significance
rs75759488117:45,000,564T/A—uncertain significance
rs1294416717:45,000,565A/C—uncertain significance
rs113169153317:45,000,566C/A—uncertain significance
rs75058943717:45,000,567C/G—likely benign
rs75627696317:45,000,568C/G—uncertain significance
rs89728164717:45,000,572T/A—uncertain significance
rs208595079817:45,000,573C/G—uncertain significance
rs214669197417:45,000,574C/T—pathogenic
rs74927015117:45,000,575A/G—conflicting classifications of pathogenicity
rs208595111617:45,000,578A/G—uncertain significance
rs127841951817:45,000,586A/G—uncertain significance
rs88603960317:45,000,588G/A—pathogenic
rs79472691517:45,000,590G/A—uncertain significance
rs57330668017:45,000,595C/T—conflicting classifications of pathogenicity
rs95192313317:45,000,596C/T—likely benign
rs74779181817:45,000,600C/T—conflicting classifications of pathogenicity
rs37439628517:45,000,602G/T—likely benign
rs95990381317:45,000,604G/A—likely benign
rs11185032217:45,000,701A/G—benign
rs1215066817:45,000,736T/C—benign
rs1085308717:45,006,112C/A——
rs143586313617:45,006,866C/T—likely benign
rs75070416317:45,006,871C/T—likely benign
rs75609809617:45,006,872T/C—likely benign
rs99332179117:45,006,874T/C—likely benign
rs214684988717:45,006,876C/T—likely benign
rs92543968217:45,006,878T/A—likely benign
rs214685010017:45,006,879T/A—likely benign
rs102759630017:45,006,882A/G—likely benign
rs214685034417:45,006,887C/G—uncertain significance
rs74787777417:45,006,895C/T—likely benign
rs11381792417:45,006,896G/A—conflicting classifications of pathogenicity
rs74668868517:45,006,903A/C—uncertain significance
rs254621441917:45,006,906C/T—uncertain significance
rs75826804517:45,006,909G/C—uncertain significance
rs77032946917:45,006,911A/G—uncertain significance
rs37486103917:45,006,912T/C—uncertain significance
rs36924792917:45,006,913G/A—uncertain significance
rs77076036617:45,006,920C/T—conflicting classifications of pathogenicity
rs20007181417:45,006,924A/G—uncertain significance
rs52893114217:45,006,927C/T—uncertain significance
rs14577288617:45,006,928G/A—likely benign
rs77354339417:45,006,933A/G—uncertain significance
rs76099750217:45,006,935A/C—uncertain significance
rs37300050117:45,006,936A/G—uncertain significance
rs146644172317:45,006,938C/T—pathogenic
rs254621508717:45,006,948A/G—uncertain significance
rs208699691517:45,006,950A/G—uncertain significance
rs156816698917:45,006,952T/G—uncertain significance
rs79605254017:45,006,954A/G—uncertain significance
rs75400438217:45,006,955G/A—uncertain significance
rs37623192317:45,006,957A/C—conflicting classifications of pathogenicity
rs36927168517:45,006,962A/G—likely benign
rs77759671017:45,006,965G/A—likely benign
rs1694128517:45,007,103T/G—benign
rs7592175717:45,007,207C/G—benign
rs207231717:45,007,213G/A—benign
rs1165566817:45,007,632A/Gintron variant—
rs11779118017:45,007,748C/Tintron variant—
rs55305449317:45,008,448T/C—likely benign
rs75261119017:45,008,458T/G—likely benign
rs134518209617:45,008,459G/T—likely benign
rs118631449617:45,008,464G/C—likely pathogenic
rs214689086717:45,008,466A/G—uncertain significance
rs155570933917:45,008,469A/G—likely benign
rs159898028417:45,008,471A/G—uncertain significance
rs208730460917:45,008,473A/G—uncertain significance
rs14896222317:45,008,474A/G—uncertain significance
rs78083214317:45,008,475C/T—likely benign
rs74553889617:45,008,476G/A—uncertain significance
rs75566217617:45,008,481C/T—likely benign
rs208730673117:45,008,491A/G—uncertain significance
rs208730701917:45,008,492T/C—uncertain significance
rs77276331917:45,008,498A/G—uncertain significance
rs106050071417:45,008,503T/C—uncertain significance
rs53411981717:45,008,506A/G—uncertain significance
rs74732825617:45,008,509C/T—uncertain significance
rs77122885517:45,008,510G/A—conflicting classifications of pathogenicity
rs14375472717:45,008,518C/T—conflicting classifications of pathogenicity
rs37776525417:45,008,519G/A—uncertain significance
rs128604101817:45,008,524G/A—uncertain significance

Showing 100 of 281 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.

GOSR2 — golgi SNAP receptor complex member 2