C7orf57

chromosome 7 open reading frame 57

Known Variants5 total

rsidPosition (GRCh37)AllelesClassClinVar
rs3749296527:48,081,032G/Auncertain significance
rs2021422997:48,083,181G/Tuncertain significance
rs102763387:48,091,847C/Tintron variant
rs7602895197:48,092,396C/Alikely benign
rs7766317517:48,092,404C/Tuncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.