C10orf53

chromosome 10 open reading frame 53

Known Variants3 total

rsidPosition (GRCh37)AllelesClassClinVar
rs57166455110:50,887,790C/Tuncertain significance
rs125826710:50,895,770G/Aintron variant
rs14788063610:50,901,862T/Guncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.