FAM228B

family with sequence similarity 228 member B

Known Variants11 total

rsidPosition (GRCh37)AllelesClassClinVar
rs5614626122:24,347,274C/A—uncertain significance
rs11947749032:24,347,306G/T—uncertain significance
rs1442312562:24,360,782C/Tsynonymous variant—
rs1887338832:24,360,829G/C—uncertain significance
rs7574556772:24,360,927G/A—uncertain significance
rs8685771312:24,362,253T/C—uncertain significance
rs5655492112:24,362,289A/G—uncertain significance
rs9336722922:24,369,671T/G—uncertain significance
rs9243966192:24,369,675G/A—uncertain significance
rs1474085652:24,369,937G/A—uncertain significance
rs7623459862:24,374,920G/T——

Gene information from NCBI Gene. Variant classifications from ClinVar.