RGMB
repulsive guidance molecule BMP co-receptor b
Summary
RGMB is a glycosylphosphatidylinositol (GPI)-anchored member of the repulsive guidance molecule family (see RGMA, MIM 607362) and contributes to the patterning of the developing nervous system (Samad et al., 2005 [PubMed 15671031]).[supplied by OMIM, Apr 2009]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2249797 | 5:98,107,341 | C/T | regulatory region variant | — |
| rs1465202304 | 5:98,109,811 | G/A | — | uncertain significance |
| rs921279140 | 5:98,109,845 | G/A | — | uncertain significance |
| rs978754868 | 5:98,109,848 | T/C | — | uncertain significance |
| rs1293482560 | 5:98,109,854 | C/T | — | uncertain significance |
| rs1289615016 | 5:98,109,857 | C/G | — | uncertain significance |
| rs926058865 | 5:98,109,859 | C/A | — | uncertain significance |
| rs1323266258 | 5:98,109,862 | C/G | — | uncertain significance |
| rs2479194339 | 5:98,115,314 | T/C | — | uncertain significance |
| rs150313779 | 5:98,115,367 | G/A | — | likely benign |
| rs764097359 | 5:98,115,493 | A/G | — | uncertain significance |
| rs778356530 | 5:98,115,535 | A/G | — | uncertain significance |
| rs199764525 | 5:98,115,542 | C/G | — | uncertain significance |
| rs760952318 | 5:98,115,677 | A/T | — | uncertain significance |
| rs2479195271 | 5:98,115,754 | C/A | — | uncertain significance |
| rs1746984114 | 5:98,128,789 | A/G | — | uncertain significance |
| rs1303272426 | 5:98,128,795 | A/G | — | uncertain significance |
| rs774998668 | 5:98,128,814 | A/G | — | likely benign |
| rs932839111 | 5:98,128,825 | G/T | — | uncertain significance |
| rs575069279 | 5:98,128,862 | C/T | — | uncertain significance |
| rs1184192871 | 5:98,129,023 | C/T | — | uncertain significance |
| rs779460504 | 5:98,129,035 | G/A | — | uncertain significance |
| rs199960380 | 5:98,129,080 | G/A | — | likely benign |
| rs143449818 | 5:98,129,105 | G/A | — | uncertain significance |
| rs779299938 | 5:98,129,110 | G/A | — | uncertain significance |
| rs373799771 | 5:98,129,116 | G/A | — | uncertain significance |
| rs2479225032 | 5:98,129,122 | G/A | — | uncertain significance |
| rs368983407 | 5:98,129,132 | C/T | — | uncertain significance |
| rs1747009040 | 5:98,129,185 | G/A | — | uncertain significance |
| rs201952910 | 5:98,129,269 | C/A | — | uncertain significance |
| rs377352086 | 5:98,129,291 | A/G | — | uncertain significance |
| rs750982179 | 5:98,129,338 | C/T | — | uncertain significance |
| rs370365109 | 5:98,129,444 | T/C | — | likely benign |
| rs1053451 | 5:98,132,052 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.