STARD9

StAR related lipid transfer domain containing 9

Summary

Enables microtubule binding activity and microtubule motor activity. Involved in spindle assembly. Located in centriole; cytoplasm; and nucleus. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants451 total

rsidPosition (GRCh37)AllelesClassClinVar
rs77073321915:42,875,566A/G—uncertain significance
rs250485370715:42,877,725A/T—uncertain significance
rs20170187315:42,877,759A/G—uncertain significance
rs18453552215:42,877,807A/G—uncertain significance
rs14503689715:42,896,996C/Tintron variant—
rs90401045615:42,930,131A/G—uncertain significance
rs74865092915:42,930,240A/G—uncertain significance
rs95186005215:42,930,270G/A—uncertain significance
rs146873099615:42,930,911T/C—uncertain significance
rs137081334415:42,930,921G/A—uncertain significance
rs99978136715:42,930,960C/G—uncertain significance
rs96804937215:42,930,972G/A—uncertain significance
rs75540368015:42,930,982G/A—likely benign
rs136649666415:42,930,999C/T—uncertain significance
rs96574794115:42,943,208C/T—likely benign
rs250542873315:42,944,768T/G—uncertain significance
rs37013048815:42,944,774C/A—uncertain significance
rs14886232915:42,953,372A/G—likely benign
rs205998663415:42,953,374C/T—uncertain significance
rs6175078815:42,953,382G/T—benign
rs54124442715:42,954,993G/A—uncertain significance
rs250553292115:42,954,999G/A—uncertain significance
rs18380273315:42,955,055C/T—likely benign
rs250553994715:42,955,490C/G—uncertain significance
rs130496587315:42,955,559T/C—uncertain significance
rs56760414215:42,955,596G/A—uncertain significance
rs127030856815:42,955,604T/C—uncertain significance
rs36993483115:42,955,652A/G—uncertain significance
rs134990058315:42,956,040C/G—uncertain significance
rs90261771615:42,956,044A/C—uncertain significance
rs140023071715:42,956,074T/C—uncertain significance
rs802490215:42,957,532T/G—benign
rs99140750115:42,958,022G/C—uncertain significance
rs91594878615:42,958,023C/A—uncertain significance
rs126794941315:42,961,434A/C—uncertain significance
rs250560839015:42,961,449G/C—uncertain significance
rs75970641115:42,961,460C/T—benign
rs77117554015:42,966,669C/T—uncertain significance
rs76432501015:42,967,085T/C—uncertain significance
rs15089839515:42,967,094G/A—benign
rs135747574115:42,967,103G/A—uncertain significance
rs120983682115:42,967,106G/C—uncertain significance
rs13942719015:42,967,111C/T—uncertain significance
rs20134644715:42,967,124A/G—benign
rs20207400715:42,967,130G/T—conflicting classifications of pathogenicity
rs15003391815:42,967,141G/T—uncertain significance
rs134148530915:42,967,151G/A—uncertain significance
rs97357714615:42,967,937G/A—uncertain significance
rs250567111815:42,967,942C/A—uncertain significance
rs76396756615:42,968,068A/T—uncertain significance
rs141365668915:42,968,071T/A—uncertain significance
rs75265649215:42,968,091C/T—uncertain significance
rs250567332215:42,968,119A/G—uncertain significance
rs57656205615:42,968,139C/T—uncertain significance
rs14436327815:42,968,140G/A—benign
rs54802690215:42,973,625C/T—likely benign
rs146023694215:42,973,661C/T—likely benign
rs75953713815:42,973,754G/A—likely benign
rs93365694715:42,974,361G/A—uncertain significance
rs77543461815:42,974,490C/T—uncertain significance
rs103499698115:42,974,529C/T—uncertain significance
rs250573210515:42,974,542C/T—uncertain significance
rs76373931215:42,974,596G/A—uncertain significance
rs18849985015:42,974,646G/A—likely benign
rs13812144015:42,974,713C/T—likely benign
rs124397531215:42,974,731G/A—uncertain significance
rs36931051115:42,976,363C/T—uncertain significance
rs250574959815:42,976,424A/G—uncertain significance
rs159576531915:42,976,435A/G—uncertain significance
rs7936560415:42,976,440G/A—likely benign
rs56333428615:42,976,447C/T—uncertain significance
rs77308430015:42,976,508C/A—uncertain significance
rs117666732315:42,976,577T/C—uncertain significance
rs14967320515:42,976,704G/A—likely benign
rs18196835615:42,976,786G/A—uncertain significance
rs250575904315:42,976,865C/G—uncertain significance
rs75694253615:42,976,964C/T—uncertain significance
rs76114456515:42,976,984A/G—uncertain significance
rs145127424315:42,976,996A/G—likely benign
rs125308343915:42,977,016G/A—uncertain significance
rs75989745215:42,977,023C/T—uncertain significance
rs159576703215:42,977,078C/T—uncertain significance
rs214022787315:42,977,099C/G—uncertain significance
rs7916589015:42,977,116T/C—likely benign
rs13980759815:42,977,198G/A—uncertain significance
rs125673581515:42,977,212C/G—uncertain significance
rs11536306515:42,977,266G/C—benign
rs52835390715:42,977,270G/A—uncertain significance
rs56432098815:42,977,275C/T—uncertain significance
rs37677174115:42,977,302A/T—uncertain significance
rs99745773215:42,977,310A/T—uncertain significance
rs53636428315:42,977,319T/C—likely benign
rs159576764215:42,977,344T/C—uncertain significance
rs7817531715:42,977,345C/T—benign
rs127478838215:42,977,365C/G—uncertain significance
rs11464398115:42,977,460C/T—benign
rs77356835515:42,977,461G/A—uncertain significance
rs104155268115:42,977,467C/A—uncertain significance
rs649305915:42,977,526A/C—benign
rs117190609315:42,977,606T/G—uncertain significance

Showing 100 of 451 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.