PSG8
pregnancy specific beta-1-glycoprotein 8
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 Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1239993591 | 19:43,258,458 | T/C | — | uncertain significance |
| rs775427803 | 19:43,258,467 | A/G | — | uncertain significance |
| rs146638942 | 19:43,258,479 | G/C | — | uncertain significance |
| rs372480345 | 19:43,258,520 | T/A | — | uncertain significance |
| rs370144520 | 19:43,258,547 | C/G | — | uncertain significance |
| rs149943830 | 19:43,258,560 | C/T | — | uncertain significance |
| rs1288395818 | 19:43,258,614 | A/G | — | uncertain significance |
| rs542714417 | 19:43,258,622 | T/C | — | uncertain significance |
| rs373734899 | 19:43,258,659 | C/A | — | uncertain significance |
| rs752870751 | 19:43,258,684 | T/A | — | uncertain significance |
| rs757765664 | 19:43,258,695 | G/T | — | uncertain significance |
| rs1969866584 | 19:43,258,712 | G/T | — | uncertain significance |
| rs1969867386 | 19:43,258,734 | G/A | — | uncertain significance |
| rs200167716 | 19:43,259,170 | G/A | — | uncertain significance |
| rs372083751 | 19:43,259,191 | T/G | — | likely benign |
| rs2513599402 | 19:43,259,218 | C/G | — | uncertain significance |
| rs746897583 | 19:43,259,262 | G/C | — | uncertain significance |
| rs113087470 | 19:43,259,265 | C/T | — | likely benign |
| rs771117205 | 19:43,259,274 | C/T | — | uncertain significance |
| rs775728209 | 19:43,259,286 | G/T | — | uncertain significance |
| rs560841302 | 19:43,259,289 | A/T | — | uncertain significance |
| rs375688393 | 19:43,259,299 | C/A | — | uncertain significance |
| rs752468754 | 19:43,259,304 | A/G | — | uncertain significance |
| rs140231543 | 19:43,259,329 | C/T | — | uncertain significance |
| rs1366363816 | 19:43,259,359 | C/T | — | uncertain significance |
| rs780177782 | 19:43,259,418 | G/A | — | uncertain significance |
| rs553846287 | 19:43,262,162 | T/C | — | uncertain significance |
| rs747553898 | 19:43,262,183 | C/T | — | uncertain significance |
| rs138487637 | 19:43,262,184 | G/A | — | uncertain significance |
| rs371313519 | 19:43,262,196 | C/G | — | uncertain significance |
| rs377706171 | 19:43,262,236 | C/A | — | uncertain significance |
| rs138201287 | 19:43,262,278 | C/G | — | uncertain significance |
| rs768840904 | 19:43,262,287 | C/G | — | uncertain significance |
| rs145990413 | 19:43,262,295 | A/T | — | uncertain significance |
| rs1278233047 | 19:43,262,322 | A/T | — | uncertain significance |
| rs116389883 | 19:43,262,361 | T/C | — | uncertain significance |
| rs751341959 | 19:43,262,366 | C/A | — | likely benign |
| rs771369931 | 19:43,262,382 | C/T | — | uncertain significance |
| rs2513607558 | 19:43,262,391 | G/T | — | uncertain significance |
| rs140758943 | 19:43,262,392 | G/C | — | uncertain significance |
| rs148041852 | 19:43,266,553 | G/T | regulatory region variant | — |
| rs201478462 | 19:43,268,061 | C/G | — | benign |
| rs895132510 | 19:43,268,113 | C/T | — | uncertain significance |
| rs148091598 | 19:43,268,119 | C/G | — | likely benign |
| rs141872267 | 19:43,268,121 | A/T | — | likely benign |
| rs146093517 | 19:43,268,122 | T/G | — | uncertain significance |
| rs138900265 | 19:43,268,126 | G/C | — | uncertain significance |
| rs79378816 | 19:43,268,153 | T/C | — | benign |
| rs751141317 | 19:43,268,196 | A/G | — | uncertain significance |
| rs1265194624 | 19:43,268,212 | T/G | — | uncertain significance |
| rs114913961 | 19:43,268,227 | A/G | — | uncertain significance |
| rs1970150215 | 19:43,268,250 | A/T | — | uncertain significance |
| rs778872603 | 19:43,268,288 | C/T | — | likely benign |
| rs750210420 | 19:43,268,289 | C/T | — | uncertain significance |
| rs570388501 | 19:43,268,302 | T/C | — | uncertain significance |
| rs201774677 | 19:43,268,311 | T/C | — | likely benign |
| rs765140265 | 19:43,268,328 | T/C | — | uncertain significance |
| rs758194328 | 19:43,268,335 | C/A | — | uncertain significance |
| rs571272164 | 19:43,268,340 | A/G | — | uncertain significance |
| rs141761918 | 19:43,268,371 | T/G | — | uncertain significance |
| rs150588080 | 19:43,268,377 | G/C | — | uncertain significance |
| rs757810717 | 19:43,268,403 | G/C | — | uncertain significance |
| rs370580594 | 19:43,268,410 | G/A | — | uncertain significance |
| rs145150049 | 19:43,268,432 | T/C | — | likely benign |
| rs1010143443 | 19:43,269,687 | T/G | — | uncertain significance |
| rs142949326 | 19:43,269,693 | G/C | — | uncertain significance |
| rs146791116 | 19:43,269,711 | G/A | — | uncertain significance |
| rs576755986 | 19:43,271,614 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.