GPR75
G protein-coupled receptor 75
Summary
GPR75 is a member of the G protein-coupled receptor family. GPRs are cell surface receptors that activate guanine-nucleotide binding proteins upon the binding of a ligand.[supplied by OMIM, Jul 2002]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201187126 | 2:54,080,276 | C/T | — | uncertain significance |
| rs376875970 | 2:54,080,279 | A/G | — | uncertain significance |
| rs994464381 | 2:54,080,437 | T/C | — | uncertain significance |
| rs1678138097 | 2:54,080,459 | T/G | — | uncertain significance |
| rs370450392 | 2:54,080,461 | C/T | — | uncertain significance |
| rs779522761 | 2:54,080,467 | T/C | — | uncertain significance |
| rs1678139419 | 2:54,080,489 | G/C | — | uncertain significance |
| rs1415078665 | 2:54,080,495 | A/T | — | uncertain significance |
| rs2528214695 | 2:54,080,524 | C/T | — | uncertain significance |
| rs199572769 | 2:54,080,572 | A/G | — | uncertain significance |
| rs2528214944 | 2:54,080,603 | A/C | — | uncertain significance |
| rs2528214998 | 2:54,080,629 | G/T | — | uncertain significance |
| rs372784242 | 2:54,080,671 | C/T | — | uncertain significance |
| rs2528215211 | 2:54,080,680 | G/C | — | uncertain significance |
| rs139789319 | 2:54,080,800 | A/G | — | uncertain significance |
| rs2528215522 | 2:54,080,801 | T/C | — | uncertain significance |
| rs138373994 | 2:54,080,850 | G/T | — | benign |
| rs746049202 | 2:54,080,893 | C/T | — | uncertain significance |
| rs762439949 | 2:54,080,917 | A/G | — | uncertain significance |
| rs537227401 | 2:54,080,989 | C/T | — | uncertain significance |
| rs373780716 | 2:54,081,037 | C/T | — | benign |
| rs148081038 | 2:54,081,198 | G/A | — | benign |
| rs1312350718 | 2:54,081,201 | C/T | — | likely benign |
| rs139723753 | 2:54,081,204 | C/T | — | likely benign |
| rs761429501 | 2:54,081,224 | T/C | — | uncertain significance |
| rs767031269 | 2:54,081,227 | T/G | — | uncertain significance |
| rs2528216837 | 2:54,081,229 | T/G | — | uncertain significance |
| rs1427973115 | 2:54,081,280 | G/T | — | uncertain significance |
| rs2528217002 | 2:54,081,290 | C/T | — | uncertain significance |
| rs144034145 | 2:54,081,348 | T/C | — | likely benign |
| rs2528217267 | 2:54,081,395 | G/A | — | uncertain significance |
| rs35349235 | 2:54,081,416 | A/C | — | benign |
| rs752397697 | 2:54,081,424 | G/A | — | uncertain significance |
| rs374900687 | 2:54,081,433 | C/A | — | uncertain significance |
| rs369270021 | 2:54,081,434 | G/A | — | uncertain significance |
| rs756619378 | 2:54,081,435 | A/T | — | uncertain significance |
| rs147684454 | 2:54,081,461 | G/A | — | uncertain significance |
| rs571785575 | 2:54,081,535 | G/C | — | uncertain significance |
| rs34000641 | 2:54,081,548 | T/C | — | benign |
| rs1421912504 | 2:54,081,618 | G/C | — | uncertain significance |
| rs2528218019 | 2:54,081,620 | A/G | — | uncertain significance |
| rs2528218200 | 2:54,081,668 | T/C | — | uncertain significance |
| rs1558629343 | 2:54,081,767 | C/T | — | uncertain significance |
| rs80328470 | 2:54,081,815 | T/C | missense variant | — |
| rs2528218619 | 2:54,081,827 | C/T | — | uncertain significance |
| rs776855671 | 2:54,081,853 | G/C | — | uncertain significance |
| rs370483316 | 2:54,081,861 | G/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.