PSG5

pregnancy specific beta-1-glycoprotein 5

Summary

The human pregnancy-specific glycoproteins (PSGs) are a group of molecules that are mainly produced by the placental syncytiotrophoblasts during pregnancy. PSGs comprise a subgroup of the carcinoembryonic antigen (CEA) family, which belongs to the immunoglobulin superfamily. For additional general information about the PSG gene family, see PSG1 (MIM 176390).[supplied by OMIM, Oct 2009]

Known Variants40 total

rsidPosition (GRCh37)AllelesClassClinVar
rs76249693819:43,674,272C/T—likely benign
rs36778325819:43,674,287G/A—uncertain significance
rs235543319:43,679,088A/T——
rs105846719:43,679,410A/G—likely benign
rs77627408019:43,679,414G/A—uncertain significance
rs15058744119:43,679,421G/A—uncertain significance
rs13964392919:43,679,430A/G—uncertain significance
rs53292382519:43,679,449C/A—uncertain significance
rs14759943119:43,679,505T/A—uncertain significance
rs77491289019:43,679,534T/C—uncertain significance
rs74637077819:43,679,537G/C—uncertain significance
rs20042449319:43,680,072C/T—uncertain significance
rs74807120719:43,680,114C/T—uncertain significance
rs14043727419:43,680,144G/A—uncertain significance
rs53636268219:43,680,168G/A—uncertain significance
rs75907870119:43,680,195A/G—uncertain significance
rs251349585919:43,680,196T/C—uncertain significance
rs76452769919:43,680,206G/C—uncertain significance
rs19950505419:43,680,215C/T—likely benign
rs20053755319:43,680,221T/G—uncertain significance
rs14246195019:43,680,235C/G—uncertain significance
rs75247677719:43,680,238A/C—likely benign
rs1042008919:43,687,770C/Tintron variant—
rs14360144819:43,688,960G/A—uncertain significance
rs74596685119:43,688,984C/T—uncertain significance
rs251351215819:43,689,047G/T—uncertain significance
rs77084079619:43,689,051C/T—uncertain significance
rs120156903619:43,689,065G/C—uncertain significance
rs53450129519:43,689,125G/A—uncertain significance
rs251351255819:43,689,142G/T—uncertain significance
rs77625276119:43,689,144C/T—uncertain significance
rs74770642719:43,689,146A/G—uncertain significance
rs76115531119:43,689,261G/C—uncertain significance
rs76208581119:43,689,269A/G—likely benign
rs20191834019:43,689,303G/A—likely benign
rs52974606919:43,690,517G/T—uncertain significance
rs37250013119:43,690,523T/C—uncertain significance
rs14233846619:43,690,527G/C—uncertain significance
rs11178036619:43,690,551G/T—uncertain significance
rs11382798019:43,692,074T/A——

Gene information from NCBI Gene. Variant classifications from ClinVar.