MYH13

myosin heavy chain 13

Summary

Predicted to enable actin filament binding activity and microfilament motor activity. Predicted to be involved in muscle contraction. Predicted to act upstream of or within cellular response to starvation. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants147 total

rsidPosition (GRCh37)AllelesClassClinVar
rs55417013417:10,204,935T/A—uncertain significance
rs57212035117:10,204,957C/T—uncertain significance
rs250787270117:10,206,574T/A—uncertain significance
rs141800640617:10,206,594G/T—uncertain significance
rs37222407817:10,206,603C/G—uncertain significance
rs76069759917:10,206,722T/C—uncertain significance
rs75855963617:10,206,725C/G—uncertain significance
rs37487420317:10,206,811C/T—uncertain significance
rs7992814217:10,206,993G/T——
rs75430011517:10,209,808C/T—uncertain significance
rs53972109917:10,209,813T/C—uncertain significance
rs18296955517:10,209,819G/A—uncertain significance
rs250787747817:10,209,858T/G—uncertain significance
rs77300611817:10,209,864G/A—uncertain significance
rs37025788217:10,209,888C/T—uncertain significance
rs76081229617:10,209,889G/A—uncertain significance
rs57401073917:10,209,916C/T—likely benign
rs19201121717:10,210,260G/A—uncertain significance
rs159788238117:10,210,318C/T—uncertain significance
rs20058136917:10,212,596C/G—uncertain significance
rs36948300117:10,212,622C/T—uncertain significance
rs14085644117:10,212,703C/T—uncertain significance
rs75469395817:10,212,709G/A—uncertain significance
rs76436388917:10,212,717T/C—conflicting classifications of pathogenicity
rs19971620017:10,212,844G/A—uncertain significance
rs55632099517:10,212,858G/A—uncertain significance
rs77528542217:10,212,901G/T—uncertain significance
rs250788266317:10,212,935C/G—uncertain significance
rs76637458517:10,212,938C/T—uncertain significance
rs19994646817:10,212,961C/A—uncertain significance
rs37428536117:10,213,002A/G—uncertain significance
rs57445508617:10,213,609T/G——
rs37226709817:10,214,487G/A—likely benign
rs119717316417:10,215,241G/T—uncertain significance
rs76706229717:10,215,248C/T—uncertain significance
rs250788768817:10,215,893T/G—uncertain significance
rs75027103417:10,215,896C/T—uncertain significance
rs54610320917:10,215,943C/T—uncertain significance
rs119286259517:10,215,965C/A—uncertain significance
rs129044064817:10,216,006G/A—uncertain significance
rs75728312017:10,216,024G/A—likely benign
rs37342593617:10,216,033G/A—uncertain significance
rs77270885117:10,216,064C/A—uncertain significance
rs75212491717:10,216,499C/T—uncertain significance
rs75546617017:10,216,500G/A—uncertain significance
rs74882088717:10,216,512C/T—uncertain significance
rs77347048517:10,216,526G/A—uncertain significance
rs19015910117:10,216,537G/A—likely benign
rs190657975917:10,216,556T/C—uncertain significance
rs20023684317:10,216,613C/T—uncertain significance
rs20173578417:10,216,635G/A—uncertain significance
rs77937116717:10,216,649G/C—uncertain significance
rs20167902217:10,216,655G/A—uncertain significance
rs76268927117:10,219,077G/A—uncertain significance
rs7281473117:10,219,097C/A—likely benign
rs77382407317:10,219,245A/G—uncertain significance
rs18250811417:10,219,261T/A—uncertain significance
rs74554084017:10,219,267G/C—uncertain significance
rs37579728517:10,219,280G/C—uncertain significance
rs20189555617:10,219,282C/T—uncertain significance
rs190669711317:10,219,308T/A—uncertain significance
rs98122755417:10,222,141A/T—uncertain significance
rs75891108817:10,222,166C/T—uncertain significance
rs56313189517:10,222,198C/T—benign
rs20206217217:10,222,215C/G—uncertain significance
rs37043228417:10,222,277C/T—uncertain significance
rs36946774617:10,222,309C/T—uncertain significance
rs78166330117:10,222,371A/T—uncertain significance
rs76752958317:10,223,525A/G—uncertain significance
rs76389209317:10,223,547G/A—uncertain significance
rs250790135617:10,223,548T/A—uncertain significance
rs20161857617:10,223,758T/C—uncertain significance
rs20087489317:10,223,782A/G—uncertain significance
rs55134152617:10,223,796C/A—uncertain significance
rs19983864517:10,224,869G/A—uncertain significance
rs159737704917:10,224,947C/G—uncertain significance
rs20060659517:10,224,960C/G—uncertain significance
rs37705623817:10,227,435A/T—uncertain significance
rs77578424217:10,227,489C/G—uncertain significance
rs76826770017:10,227,493G/A—uncertain significance
rs75403295517:10,227,565A/C—uncertain significance
rs250791393917:10,231,289C/T—uncertain significance
rs77533501217:10,231,314C/A—uncertain significance
rs123657163017:10,231,316A/T—uncertain significance
rs95893026517:10,231,336A/T—uncertain significance
rs19951911817:10,231,337C/T—uncertain significance
rs20164480217:10,231,340T/C—uncertain significance
rs76374124817:10,231,394T/C—uncertain significance
rs250791421717:10,231,410T/C—uncertain significance
rs75327681217:10,233,725A/C—uncertain significance
rs77455771317:10,233,764G/A—uncertain significance
rs36991976017:10,235,454C/T—uncertain significance
rs250791899717:10,235,465A/G—uncertain significance
rs75913723117:10,235,534C/T—uncertain significance
rs90259018117:10,236,392G/A—uncertain significance
rs97573496517:10,236,430C/A—uncertain significance
rs139413990017:10,236,448A/T—uncertain significance
rs250792026217:10,236,466T/C—uncertain significance
rs75394174317:10,243,484T/C—uncertain significance
rs54668986317:10,243,488G/A—uncertain significance

Showing 100 of 147 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.