FAM228B

family with sequence similarity 228 member B

Known Variants11 total

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

Gene information from NCBI Gene. Variant classifications from ClinVar.