GPR156
G protein-coupled receptor 156
Summary
G protein-coupled receptors (GPCRs) are a large superfamily of cell surface receptors characterized by 7 helical transmembrane domains, together with N-terminal extracellular and C-terminal intracellular domains.[supplied by OMIM, Mar 2008]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs370861924 | 3:119,886,023 | G/C | — | uncertain significance |
| rs755257511 | 3:119,886,045 | C/T | — | uncertain significance |
| rs1029465170 | 3:119,886,058 | A/G | — | uncertain significance |
| rs371829132 | 3:119,886,082 | A/C | — | uncertain significance |
| rs769461698 | 3:119,886,090 | T/C | — | uncertain significance |
| rs573111287 | 3:119,886,135 | A/C | — | likely benign |
| rs1383829072 | 3:119,886,142 | G/T | — | uncertain significance |
| rs376022438 | 3:119,886,157 | G/C | — | uncertain significance |
| rs757734122 | 3:119,886,172 | G/A | — | uncertain significance |
| rs367758171 | 3:119,886,204 | C/T | — | uncertain significance |
| rs773739887 | 3:119,886,208 | G/C | — | uncertain significance |
| rs775719509 | 3:119,886,235 | G/A | — | uncertain significance |
| rs1294613814 | 3:119,886,243 | G/A | — | uncertain significance |
| rs768056878 | 3:119,886,268 | C/T | — | uncertain significance |
| rs2546012256 | 3:119,886,394 | T/G | — | uncertain significance |
| rs1443550271 | 3:119,886,405 | C/A | — | uncertain significance |
| rs148653681 | 3:119,886,457 | G/A | — | uncertain significance |
| rs1304435329 | 3:119,886,466 | C/T | — | uncertain significance |
| rs1256906132 | 3:119,886,495 | G/A | — | uncertain significance |
| rs376129523 | 3:119,886,498 | C/T | — | uncertain significance |
| rs375975333 | 3:119,886,528 | A/C | — | uncertain significance |
| rs762670033 | 3:119,886,622 | G/C | — | uncertain significance |
| rs750261430 | 3:119,886,646 | G/C | — | uncertain significance |
| rs775980033 | 3:119,886,711 | C/T | — | likely benign |
| rs139771398 | 3:119,886,714 | C/T | — | uncertain significance |
| rs575756351 | 3:119,886,715 | G/A | — | uncertain significance |
| rs2546013678 | 3:119,886,852 | G/A | — | uncertain significance |
| rs143279740 | 3:119,887,002 | C/T | — | likely benign |
| rs772410934 | 3:119,887,096 | C/T | — | likely benign |
| rs113424982 | 3:119,887,107 | G/C | — | uncertain significance |
| rs745532011 | 3:119,887,197 | A/C | — | uncertain significance |
| rs561396784 | 3:119,892,182 | A/T | — | uncertain significance |
| rs562535511 | 3:119,892,199 | G/A | — | likely benign |
| rs779642936 | 3:119,892,225 | C/G | — | uncertain significance |
| rs139943256 | 3:119,892,232 | T/C | — | uncertain significance |
| rs199542673 | 3:119,892,255 | G/C | — | uncertain significance |
| rs770043908 | 3:119,892,269 | T/C | — | uncertain significance |
| rs745703715 | 3:119,900,115 | C/A | — | uncertain significance |
| rs2546027740 | 3:119,900,153 | G/A | — | uncertain significance |
| rs747449215 | 3:119,900,155 | G/T | — | uncertain significance |
| rs151169068 | 3:119,904,174 | A/G | — | uncertain significance |
| rs145207432 | 3:119,904,187 | G/A | — | likely benign |
| rs776561802 | 3:119,905,505 | C/T | — | pathogenic |
| rs1279244104 | 3:119,905,512 | C/A | — | uncertain significance |
| rs1195382418 | 3:119,905,540 | T/A | — | uncertain significance |
| rs2059038829 | 3:119,905,555 | C/G | — | uncertain significance |
| rs2546032459 | 3:119,905,621 | C/A | — | uncertain significance |
| rs1353746216 | 3:119,911,842 | C/T | — | uncertain significance |
| rs779056618 | 3:119,912,171 | C/T | — | uncertain significance |
| rs1276974684 | 3:119,912,200 | G/A | — | uncertain significance |
| rs912890903 | 3:119,912,207 | T/G | — | uncertain significance |
| rs545230660 | 3:119,924,079 | A/G | — | — |
| rs35902169 | 3:119,926,380 | A/T | upstream gene variant | — |
| rs957346927 | 3:119,962,592 | G/C | — | uncertain significance |
| rs2546078861 | 3:119,962,593 | A/C | — | uncertain significance |
| rs1298633721 | 3:119,962,878 | G/T | — | uncertain significance |
| rs772984135 | 3:119,962,895 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.