RHBG
Rh family B glycoprotein
Summary
This gene encodes one of two non-erythroid members of the Rhesus (Rh) protein family. Non-erythroid Rh protein family members are mainly expressed in the kidney and belong to the methylammonium-ammonium permease/ammonia transporters superfamily. All Rh family proteins are predicted to be transmembrane proteins with 12 membrane spanning domains and intracytoplasmic N- and C-termini. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201291978 | 1:156,339,047 | G/C | — | uncertain significance |
| rs745614758 | 1:156,339,098 | C/T | — | uncertain significance |
| rs375087227 | 1:156,339,143 | C/T | — | uncertain significance |
| rs2525417352 | 1:156,339,170 | C/G | — | uncertain significance |
| rs7525133 | 1:156,341,494 | G/T | — | — |
| rs75348726 | 1:156,346,665 | C/A | intron variant | — |
| rs972886958 | 1:156,347,101 | A/G | — | uncertain significance |
| rs1667279562 | 1:156,347,133 | T/G | — | uncertain significance |
| rs200069134 | 1:156,347,160 | G/A | — | uncertain significance |
| rs79075455 | 1:156,347,809 | G/A | — | uncertain significance |
| rs775445928 | 1:156,347,815 | C/G | — | uncertain significance |
| rs2525463159 | 1:156,347,878 | C/A | — | uncertain significance |
| rs930410306 | 1:156,348,067 | A/T | — | uncertain significance |
| rs2525466205 | 1:156,348,080 | T/G | — | uncertain significance |
| rs537105074 | 1:156,348,106 | T/C | — | uncertain significance |
| rs267598074 | 1:156,348,107 | C/T | — | uncertain significance |
| rs760016272 | 1:156,351,212 | A/T | — | uncertain significance |
| rs756706384 | 1:156,351,216 | C/T | — | uncertain significance |
| rs778886045 | 1:156,351,616 | C/T | — | uncertain significance |
| rs776985894 | 1:156,351,659 | G/A | — | uncertain significance |
| rs1338984687 | 1:156,351,690 | T/A | — | uncertain significance |
| rs200378283 | 1:156,351,733 | C/T | — | uncertain significance |
| rs781335209 | 1:156,351,934 | G/A | — | uncertain significance |
| rs376569860 | 1:156,351,953 | T/C | — | uncertain significance |
| rs1174572610 | 1:156,351,988 | G/A | — | uncertain significance |
| rs769518777 | 1:156,352,562 | T/C | — | uncertain significance |
| rs1209119890 | 1:156,352,567 | G/C | — | uncertain significance |
| rs1352296583 | 1:156,352,574 | A/G | — | uncertain significance |
| rs750840184 | 1:156,352,612 | G/A | — | uncertain significance |
| rs151015551 | 1:156,352,648 | G/C | — | uncertain significance |
| rs774132018 | 1:156,352,651 | G/A | — | likely benign |
| rs776725986 | 1:156,352,658 | G/A | — | uncertain significance |
| rs367749889 | 1:156,354,329 | A/G | — | uncertain significance |
| rs375620360 | 1:156,354,355 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.