CGB8

chorionic gonadotropin subunit beta 8

Summary

This gene is a member of the glycoprotein hormone beta chain family and encodes the beta 8 subunit of chorionic gonadotropin (CG). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biological specificity. CG is produced by the trophoblastic cells of the placenta and stimulates the ovaries to synthesize the steroids that are essential for the maintenance of pregnancy. The beta subunit of CG is encoded by 6 genes which are arranged in tandem and inverted pairs on chromosome 19q13.3 and contiguous with the luteinizing hormone beta subunit gene. [provided by RefSeq, Jul 2008]

Known Variants24 total

rsidPosition (GRCh37)AllelesClassClinVar
rs75825356119:49,550,928G/C—uncertain significance
rs7135272619:49,550,960A/T—uncertain significance
rs121427377419:49,550,997G/A—uncertain significance
rs76110871719:49,551,009C/G—uncertain significance
rs91515848219:49,551,036T/A—uncertain significance
rs251382751519:49,551,054T/G—uncertain significance
rs140826810819:49,551,085G/C—uncertain significance
rs135422127719:49,551,124C/A—uncertain significance
rs125909785419:49,551,129C/T—uncertain significance
rs87987153019:49,551,132G/A—uncertain significance
rs92775016919:49,551,171C/T—uncertain significance
rs141437248619:49,551,177T/G—likely benign
rs133843916919:49,551,187C/T—uncertain significance
rs119949901019:49,551,210C/G—likely benign
rs136857610919:49,551,220C/T—uncertain significance
rs146396436119:49,551,464T/C—uncertain significance
rs137551278319:49,551,562C/T—uncertain significance
rs125272758019:49,551,568C/T—uncertain significance
rs395624819:49,551,574G/A—uncertain significance
rs251382814219:49,551,604C/T—uncertain significance
rs20025241619:49,551,628C/T—uncertain significance
rs37507995419:49,551,987A/C—uncertain significance
rs54398559419:49,551,989A/G—uncertain significance
rs2855391919:49,553,380A/Cdownstream gene variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.