RUNDC3B
RUN domain containing 3B
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1820882048 | 7:87,258,177 | G/C | — | uncertain significance |
| rs2547022723 | 7:87,258,179 | G/A | — | uncertain significance |
| rs545028126 | 7:87,258,182 | G/A | — | uncertain significance |
| rs2547061244 | 7:87,280,233 | T/G | — | uncertain significance |
| rs200940747 | 7:87,323,273 | A/T | — | uncertain significance |
| rs545413671 | 7:87,329,769 | C/T | — | uncertain significance |
| rs750107326 | 7:87,329,803 | G/A | — | uncertain significance |
| rs751080320 | 7:87,329,827 | G/A | — | uncertain significance |
| rs769745143 | 7:87,339,891 | A/T | — | uncertain significance |
| rs2547160985 | 7:87,339,968 | C/A | — | uncertain significance |
| rs549915041 | 7:87,355,769 | A/G | — | — |
| rs114137957 | 7:87,374,869 | T/G | intron variant | — |
| rs180754372 | 7:87,384,159 | A/G | intron variant | — |
| rs74814100 | 7:87,395,427 | C/T | intron variant | — |
| rs186576644 | 7:87,398,254 | T/C | intron variant | — |
| rs778964395 | 7:87,399,980 | G/T | — | uncertain significance |
| rs1008097444 | 7:87,400,037 | A/T | — | uncertain significance |
| rs147737258 | 7:87,400,041 | G/C | — | uncertain significance |
| rs760764597 | 7:87,407,207 | G/A | — | uncertain significance |
| rs1029421 | 7:87,418,861 | T/G | — | — |
| rs752473237 | 7:87,436,720 | G/A | — | uncertain significance |
| rs1325060127 | 7:87,436,741 | T/C | — | uncertain significance |
| rs150419056 | 7:87,436,815 | C/G | — | uncertain significance |
| rs1429419729 | 7:87,445,472 | C/T | — | uncertain significance |
| rs201766719 | 7:87,445,496 | A/G | — | uncertain significance |
| rs756454514 | 7:87,445,508 | A/G | — | uncertain significance |
| rs768751804 | 7:87,445,542 | A/T | — | uncertain significance |
| rs761836205 | 7:87,459,272 | C/G | — | uncertain significance |
| rs575156411 | 7:87,461,917 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.