ADARB2
adenosine deaminase RNA specific B2 (inactive)
Summary
This gene encodes a member of the double-stranded RNA adenosine deaminase family of RNA-editing enzymes and may play a regulatory role in RNA editing. [provided by RefSeq, Jul 2008]
Known Variants86 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1836704133 | 10:1,229,152 | T/A | — | uncertain significance |
| rs773347607 | 10:1,229,165 | G/A | — | uncertain significance |
| rs2490908374 | 10:1,229,249 | C/G | — | uncertain significance |
| rs2490908425 | 10:1,229,285 | C/T | — | uncertain significance |
| rs138438667 | 10:1,229,299 | C/T | — | uncertain significance |
| rs202198509 | 10:1,230,814 | C/T | — | uncertain significance |
| rs369823256 | 10:1,230,815 | G/A | — | uncertain significance |
| rs143420247 | 10:1,230,823 | C/T | — | uncertain significance |
| rs746757303 | 10:1,230,842 | T/G | — | uncertain significance |
| rs141298814 | 10:1,230,874 | C/T | — | benign |
| rs373191144 | 10:1,230,943 | G/A | — | uncertain significance |
| rs762464849 | 10:1,230,961 | G/A | — | uncertain significance |
| rs4880785 | 10:1,237,920 | A/G | intron variant | — |
| rs773372364 | 10:1,245,938 | G/A | — | uncertain significance |
| rs369397900 | 10:1,245,939 | C/G | — | uncertain significance |
| rs4880487 | 10:1,246,883 | C/T | intron variant | — |
| rs1241773933 | 10:1,262,984 | A/G | — | uncertain significance |
| rs747329974 | 10:1,263,026 | C/T | — | uncertain significance |
| rs184297552 | 10:1,263,027 | G/C | — | uncertain significance |
| rs138734198 | 10:1,263,039 | C/T | — | uncertain significance |
| rs544133389 | 10:1,263,815 | C/T | — | — |
| rs1425606361 | 10:1,279,641 | G/C | — | uncertain significance |
| rs1830831663 | 10:1,279,666 | G/A | — | uncertain significance |
| rs35356097 | 10:1,279,760 | C/T | — | benign |
| rs149857202 | 10:1,279,779 | C/T | — | uncertain significance |
| rs199735124 | 10:1,279,780 | G/T | — | uncertain significance |
| rs142949222 | 10:1,284,228 | G/T | — | uncertain significance |
| rs1332817425 | 10:1,284,242 | C/T | — | uncertain significance |
| rs201639089 | 10:1,284,249 | C/T | — | uncertain significance |
| rs761373140 | 10:1,284,257 | G/A | — | uncertain significance |
| rs374032478 | 10:1,284,300 | C/T | — | uncertain significance |
| rs200534087 | 10:1,284,336 | C/T | — | uncertain significance |
| rs551961865 | 10:1,284,355 | A/G | — | likely benign |
| rs538734059 | 10:1,284,357 | C/T | — | uncertain significance |
| rs780188177 | 10:1,313,162 | C/T | — | uncertain significance |
| rs144565549 | 10:1,313,185 | C/T | — | uncertain significance |
| rs770421331 | 10:1,313,186 | G/C | — | uncertain significance |
| rs765800300 | 10:1,313,209 | G/A | — | likely benign |
| rs765731656 | 10:1,313,219 | C/T | — | uncertain significance |
| rs201071907 | 10:1,313,220 | G/A | — | benign |
| rs146672392 | 10:1,313,222 | G/A | — | uncertain significance |
| rs200545586 | 10:1,313,258 | C/T | — | uncertain significance |
| rs11599315 | 10:1,343,017 | C/T | intron variant | — |
| rs2805533 | 10:1,384,633 | G/A | intron variant | — |
| rs566838000 | 10:1,405,245 | G/C | — | uncertain significance |
| rs1369088145 | 10:1,405,254 | G/A | — | uncertain significance |
| rs1386040782 | 10:1,405,264 | C/T | — | uncertain significance |
| rs368208673 | 10:1,405,316 | C/T | — | benign |
| rs191180422 | 10:1,405,402 | C/T | — | benign |
| rs1264212022 | 10:1,405,500 | G/A | — | uncertain significance |
| rs967357807 | 10:1,405,524 | C/T | — | likely benign |
| rs1180210627 | 10:1,405,525 | G/A | — | uncertain significance |
| rs981640528 | 10:1,405,539 | C/G | — | uncertain significance |
| rs960748032 | 10:1,405,546 | C/T | — | likely benign |
| rs916686150 | 10:1,405,575 | C/T | — | uncertain significance |
| rs1282711394 | 10:1,405,646 | A/C | — | uncertain significance |
| rs892922595 | 10:1,405,716 | G/A | — | uncertain significance |
| rs1832283581 | 10:1,405,807 | G/A | — | uncertain significance |
| rs35398040 | 10:1,405,835 | G/A | — | benign |
| rs751727246 | 10:1,405,845 | T/G | — | uncertain significance |
| rs746391870 | 10:1,405,857 | G/A | — | uncertain significance |
| rs1832284616 | 10:1,405,872 | C/T | — | uncertain significance |
| rs377136355 | 10:1,405,873 | G/C | — | uncertain significance |
| rs1347596088 | 10:1,405,887 | G/C | — | uncertain significance |
| rs143914218 | 10:1,405,925 | C/T | — | likely benign |
| rs749722366 | 10:1,405,936 | A/G | — | uncertain significance |
| rs1588233082 | 10:1,405,995 | A/C | — | uncertain significance |
| rs1832286804 | 10:1,406,004 | T/G | — | uncertain significance |
| rs1225574207 | 10:1,406,032 | G/A | — | uncertain significance |
| rs200348424 | 10:1,406,037 | C/G | — | uncertain significance |
| rs1429405968 | 10:1,406,052 | G/A | — | likely benign |
| rs11250464 | 10:1,406,364 | T/C | regulatory region variant | — |
| rs908831986 | 10:1,421,278 | C/T | — | uncertain significance |
| rs182864478 | 10:1,421,340 | A/G | — | uncertain significance |
| rs1832460097 | 10:1,421,344 | T/C | — | uncertain significance |
| rs17293817 | 10:1,452,786 | G/A | intron variant | — |
| rs2820651 | 10:1,471,765 | C/A | intron variant | — |
| rs550403877 | 10:1,522,806 | T/A | — | — |
| rs2999399 | 10:1,630,821 | C/A | — | — |
| rs573363703 | 10:1,651,480 | C/T | — | — |
| rs6560749 | 10:1,676,531 | T/G | intron variant | — |
| rs77027562 | 10:1,730,938 | A/G | intron variant | — |
| rs756031726 | 10:1,779,268 | C/T | — | uncertain significance |
| rs770999496 | 10:1,779,301 | C/T | — | uncertain significance |
| rs763896714 | 10:1,779,322 | C/A | — | uncertain significance |
| rs756931124 | 10:1,779,328 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.