ORM2
orosomucoid 2
Summary
This gene encodes a key acute phase plasma protein. Because of its increase due to acute inflammation, this protein is classified as an acute-phase reactant. The specific function of this protein has not yet been determined; however, it may be involved in aspects of immunosuppression. [provided by RefSeq, Jul 2008]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3762056 | 9:117,090,434 | C/T | upstream gene variant | — |
| rs3762055 | 9:117,090,575 | T/C | regulatory region variant | — |
| rs10982164 | 9:117,091,067 | G/A | regulatory region variant | — |
| rs7040440 | 9:117,091,074 | C/T | regulatory region variant | — |
| rs142414765 | 9:117,092,020 | G/C | — | — |
| rs768724177 | 9:117,092,189 | C/T | — | uncertain significance |
| rs143336597 | 9:117,092,203 | C/T | — | likely benign |
| rs774274413 | 9:117,092,233 | G/A | — | uncertain significance |
| rs755873204 | 9:117,092,263 | G/C | — | uncertain significance |
| rs748201206 | 9:117,092,284 | G/A | — | uncertain significance |
| rs370008862 | 9:117,092,296 | C/T | — | likely benign |
| rs201562247 | 9:117,092,756 | G/A | — | uncertain significance |
| rs2490488105 | 9:117,092,786 | C/G | — | uncertain significance |
| rs149310648 | 9:117,093,115 | C/T | — | uncertain significance |
| rs760081372 | 9:117,093,902 | G/C | — | likely benign |
| rs78377107 | 9:117,093,923 | C/T | — | likely benign |
| rs142563384 | 9:117,094,149 | C/T | — | benign |
| rs148221879 | 9:117,094,159 | G/C | — | uncertain significance |
| rs1214997559 | 9:117,094,162 | T/G | — | uncertain significance |
| rs149574658 | 9:117,094,207 | A/C | — | uncertain significance |
| rs113229705 | 9:117,094,854 | C/T | downstream gene variant | — |
| rs1687417 | 9:117,095,146 | T/G | downstream gene variant | — |
| rs1829888432 | 9:117,095,373 | C/A | — | uncertain significance |
| rs565103849 | 9:117,095,379 | G/A | — | uncertain significance |
| rs2490500090 | 9:117,095,404 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.