C7orf57

chromosome 7 open reading frame 57

Known Variants5 total

rsidPosition (GRCh37)AllelesClassClinVar
rs3749296527:48,081,032G/A—uncertain significance
rs2021422997:48,083,181G/T—uncertain significance
rs102763387:48,091,847C/Tintron variant—
rs7602895197:48,092,396C/A—likely benign
rs7766317517:48,092,404C/T—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.