DONSON

DNA replication fork stabilization factor DONSON

Summary

This gene lies downstream of the SON gene and spans 10 kb on chromosome 21. The function of this gene is unknown. [provided by RefSeq, Jul 2008]

Known Variants186 total

rsidPosition (GRCh37)AllelesClassClinVar
rs11646192121:34,950,609A/G—benign
rs251746507721:34,950,640T/C—likely benign
rs76504532621:34,950,643C/T—likely benign
rs74993733021:34,950,644A/C—uncertain significance
rs74863725021:34,950,656C/T—uncertain significance
rs11355334721:34,950,657G/A—uncertain significance
rs77461657321:34,950,680G/A—pathogenic
rs14752158421:34,950,699C/T—likely benign
rs136922853321:34,950,722C/G—uncertain significance
rs14123731221:34,950,728G/A—likely benign
rs144563470821:34,950,742A/G—likely benign
rs121333589721:34,950,762T/C—likely benign
rs137374727721:34,950,768C/A—likely benign
rs76271290721:34,951,636G/A—likely benign
rs91321263921:34,951,637C/G—likely benign
rs53429929821:34,951,655C/A—pathogenic
rs20148732321:34,951,657A/T—likely benign
rs14501482421:34,951,673C/G—likely benign
rs76201612521:34,951,695T/A—likely benign
rs37468852721:34,951,709C/T—uncertain significance
rs36846934221:34,951,710G/A—likely benign
rs214589917521:34,951,739C/T—uncertain significance
rs14666403621:34,951,753T/G—conflicting classifications of pathogenicity
rs78010496321:34,951,763T/C—uncertain significance
rs75183639521:34,951,767C/T—uncertain significance
rs54463895921:34,951,775G/A—conflicting classifications of pathogenicity
rs37212668621:34,951,786G/A—pathogenic
rs14059243421:34,951,808C/T—conflicting classifications of pathogenicity
rs140815022621:34,951,818T/C—likely benign
rs95984354521:34,951,829A/G—uncertain significance
rs19077344121:34,951,831C/A—benign
rs133162136821:34,951,846G/C—uncertain significance
rs13945121121:34,951,848C/T—benign
rs76679042121:34,951,864C/A—uncertain significance
rs75167553921:34,951,865G/A—uncertain significance
rs19956352221:34,951,880T/C—likely benign
rs283423821:34,952,008G/A—benign
rs76353119521:34,953,593G/A—likely benign
rs76658739521:34,953,602T/A—uncertain significance
rs75905064421:34,953,617T/C—likely benign
rs13833519821:34,953,618T/C—uncertain significance
rs113540195921:34,953,621A/G—pathogenic
rs75364804821:34,953,634G/A—pathogenic
rs14918383621:34,953,672G/T—uncertain significance
rs99368702921:34,953,676G/Astop gainedpathogenic
rs251747070021:34,953,728T/C—likely benign
rs77477326221:34,953,730T/C—uncertain significance
rs75039086821:34,953,804C/T—uncertain significance
rs20092323621:34,953,809G/A—uncertain significance
rs283423921:34,954,156G/A—benign
rs6222771021:34,954,170G/A—benign
rs75030076821:34,954,239C/G—likely benign
rs251747165621:34,954,262G/C—uncertain significance
rs54988250021:34,954,264T/C—uncertain significance
rs37326281821:34,954,273T/C—uncertain significance
rs78075149721:34,954,349G/A—likely benign
rs74734185421:34,954,352G/A—likely benign
rs14915860021:34,954,360C/G—uncertain significance
rs77914968121:34,954,370T/Cdownstream gene variantpathogenic
rs75531095221:34,954,463T/C—likely benign
rs208651933421:34,954,469A/G—likely pathogenic
rs36857017621:34,954,485G/A—uncertain significance
rs14646184821:34,954,486C/G—uncertain significance
rs19998967721:34,954,518A/T—uncertain significance
rs54886671721:34,954,527T/G—likely benign
rs132222556921:34,954,538G/C—uncertain significance
rs76056440021:34,954,555A/G—benign
rs56969276221:34,954,558T/G—likely benign
rs53707188621:34,954,559G/A—likely benign
rs75357200021:34,954,565C/T—uncertain significance
rs52804532021:34,955,494G/A——
rs18795936721:34,955,781C/T—likely benign
rs77636567421:34,955,784A/C—likely benign
rs140034073521:34,955,785A/C—likely benign
rs208654110021:34,955,802C/G—uncertain significance
rs138848071221:34,955,820C/T—uncertain significance
rs76257514821:34,955,837T/C—uncertain significance
rs14630100021:34,955,839T/C—uncertain significance
rs75642563721:34,955,842G/A—uncertain significance
rs14809511221:34,955,866C/A—uncertain significance
rs251747497021:34,955,873T/C—likely benign
rs54229698221:34,955,881G/A—pathogenic
rs77980344721:34,955,882G/Cmissense variantpathogenic
rs98181305321:34,955,911C/T—uncertain significance
rs142453047921:34,955,919T/C—uncertain significance
rs14711571121:34,955,922G/A—uncertain significance
rs37457017921:34,955,948A/G—likely benign
rs36790475921:34,955,949T/C—conflicting classifications of pathogenicity
rs208654338721:34,955,960A/G—likely benign
rs20216828221:34,955,979A/G—conflicting classifications of pathogenicity
rs37359755921:34,955,980G/A—likely benign
rs113540196021:34,955,994T/C—conflicting classifications of pathogenicity
rs19258555221:34,956,005T/C—no classification for the single variant
rs76656680721:34,956,919C/T—likely benign
rs6174611921:34,956,929T/C—conflicting classifications of pathogenicity
rs75515106221:34,956,930C/T—uncertain significance
rs74811857621:34,956,937C/T—pathogenic
rs75580887621:34,956,947G/A—uncertain significance
rs74910829921:34,956,953C/T—uncertain significance
rs208655765421:34,956,957C/T—likely benign

Showing 100 of 186 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.