APOBR
apolipoprotein B receptor
Summary
Apolipoprotein B48 receptor is a macrophage receptor that binds to the apolipoprotein B48 of dietary triglyceride (TG)-rich lipoproteins. This receptor may provide essential lipids, lipid-soluble vitamins and other nutrients to reticuloendothelial cells. If overwhelmed with elevated plasma triglyceride, the apolipoprotein B48 receptor may contribute to foam cell formation, endothelial dysfunction, and atherothrombogenesis. [provided by RefSeq, Jul 2008]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs528796656 | 16:28,506,049 | G/C | — | uncertain significance |
| rs577322366 | 16:28,506,429 | G/C | — | uncertain significance |
| rs750357089 | 16:28,506,465 | C/A | — | uncertain significance |
| rs1368281057 | 16:28,506,672 | G/A | — | uncertain significance |
| rs2506559005 | 16:28,506,811 | A/G | — | likely benign |
| rs752397580 | 16:28,506,845 | G/C | — | uncertain significance |
| rs2506559961 | 16:28,506,972 | G/A | — | likely benign |
| rs578246087 | 16:28,506,979 | C/T | — | uncertain significance |
| rs1047786311 | 16:28,507,003 | G/A | — | uncertain significance |
| rs986738399 | 16:28,507,084 | C/G | — | uncertain significance |
| rs766539785 | 16:28,507,090 | G/A | — | uncertain significance |
| rs1451518545 | 16:28,507,132 | G/T | — | uncertain significance |
| rs757964944 | 16:28,507,197 | G/A | — | uncertain significance |
| rs971018613 | 16:28,507,307 | C/A | — | likely benign |
| rs542615363 | 16:28,507,308 | G/A | — | likely benign |
| rs773667784 | 16:28,507,347 | G/A | — | uncertain significance |
| rs62034289 | 16:28,507,378 | T/C | — | likely benign |
| rs62034313 | 16:28,507,397 | T/C | — | likely benign |
| rs1464611386 | 16:28,507,425 | G/A | — | uncertain significance |
| rs180743 | 16:28,507,644 | C/T | missense variant | — |
| rs62034316 | 16:28,507,916 | C/T | — | likely benign |
| rs201285042 | 16:28,508,094 | G/A | — | likely benign |
| rs772513637 | 16:28,508,258 | G/A | — | uncertain significance |
| rs754869005 | 16:28,508,295 | G/A | — | uncertain significance |
| rs2506568991 | 16:28,508,352 | G/A | — | uncertain significance |
| rs2506570308 | 16:28,508,550 | G/C | — | uncertain significance |
| rs1210178074 | 16:28,508,630 | G/T | — | uncertain significance |
| rs1332779093 | 16:28,508,635 | G/A | — | uncertain significance |
| rs377073634 | 16:28,508,667 | G/A | — | uncertain significance |
| rs746573798 | 16:28,508,758 | C/T | — | likely benign |
| rs2506572132 | 16:28,508,768 | G/T | — | uncertain significance |
| rs113343275 | 16:28,508,782 | A/C | — | benign |
| rs1193081979 | 16:28,508,854 | C/T | — | likely benign |
| rs1252436163 | 16:28,509,420 | C/T | — | uncertain significance |
| rs2506576762 | 16:28,509,424 | T/C | — | uncertain significance |
| rs2506578063 | 16:28,509,610 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.