NRDE2
NRDE-2, necessary for RNA interference, domain containing
Summary
Involved in several processes, including RNA splicing; mRNA stabilization; and positive regulation of RNA export from nucleus. Located in nuclear speck and nucleolus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants86 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2503983316 | 14:90,744,724 | C/A | — | uncertain significance |
| rs748554252 | 14:90,744,730 | G/A | — | uncertain significance |
| rs377201570 | 14:90,744,772 | C/T | — | uncertain significance |
| rs201062537 | 14:90,744,776 | G/T | — | uncertain significance |
| rs139694903 | 14:90,744,787 | C/T | — | uncertain significance |
| rs776488985 | 14:90,744,790 | C/T | — | uncertain significance |
| rs756889173 | 14:90,745,473 | G/A | — | uncertain significance |
| rs2503996947 | 14:90,752,729 | G/T | — | uncertain significance |
| rs376798752 | 14:90,752,748 | C/T | — | uncertain significance |
| rs567915458 | 14:90,752,800 | C/G | — | uncertain significance |
| rs11626933 | 14:90,754,311 | A/G | intron variant | — |
| rs1283205484 | 14:90,754,649 | T/C | — | likely benign |
| rs775950590 | 14:90,754,658 | A/G | — | uncertain significance |
| rs201946043 | 14:90,754,711 | G/T | — | uncertain significance |
| rs201095043 | 14:90,754,756 | G/A | — | uncertain significance |
| rs149143718 | 14:90,754,768 | C/T | — | uncertain significance |
| rs563096641 | 14:90,754,840 | G/C | — | uncertain significance |
| rs143522507 | 14:90,754,886 | C/G | — | uncertain significance |
| rs570825290 | 14:90,754,918 | A/G | — | uncertain significance |
| rs59039343 | 14:90,754,937 | C/T | — | benign |
| rs2504001549 | 14:90,754,975 | T/C | — | uncertain significance |
| rs142250129 | 14:90,755,015 | G/A | — | likely benign |
| rs183000861 | 14:90,755,027 | C/T | — | uncertain significance |
| rs533874068 | 14:90,755,143 | T/C | — | likely benign |
| rs151274632 | 14:90,755,145 | G/A | — | likely benign |
| rs745848812 | 14:90,755,147 | G/C | — | uncertain significance |
| rs766936764 | 14:90,755,186 | G/C | — | uncertain significance |
| rs753974189 | 14:90,755,191 | G/A | — | uncertain significance |
| rs2504002289 | 14:90,755,236 | G/C | — | uncertain significance |
| rs766846805 | 14:90,755,264 | C/G | — | uncertain significance |
| rs375535926 | 14:90,755,383 | T/C | — | uncertain significance |
| rs368549011 | 14:90,755,401 | T/A | — | uncertain significance |
| rs1595059617 | 14:90,756,572 | A/G | — | uncertain significance |
| rs913260111 | 14:90,756,603 | G/C | — | uncertain significance |
| rs185017125 | 14:90,756,639 | G/A | — | uncertain significance |
| rs2504005286 | 14:90,756,693 | A/C | — | uncertain significance |
| rs141706947 | 14:90,756,699 | G/A | — | uncertain significance |
| rs150533632 | 14:90,756,720 | G/A | — | uncertain significance |
| rs147436404 | 14:90,756,819 | G/C | — | uncertain significance |
| rs1014874218 | 14:90,756,935 | A/G | — | uncertain significance |
| rs2282032 | 14:90,758,891 | G/T | intron variant | — |
| rs770807341 | 14:90,759,070 | C/T | — | uncertain significance |
| rs368425343 | 14:90,759,097 | G/A | — | uncertain significance |
| rs750534213 | 14:90,759,102 | G/A | — | uncertain significance |
| rs769347186 | 14:90,759,129 | C/T | — | uncertain significance |
| rs2503346402 | 14:90,759,142 | G/A | — | uncertain significance |
| rs146810395 | 14:90,764,612 | A/C | — | uncertain significance |
| rs368842771 | 14:90,764,685 | G/A | — | uncertain significance |
| rs764247349 | 14:90,764,688 | G/T | — | uncertain significance |
| rs922345858 | 14:90,764,703 | A/G | — | uncertain significance |
| rs201603043 | 14:90,764,709 | G/T | — | uncertain significance |
| rs754913653 | 14:90,764,724 | C/A | — | uncertain significance |
| rs2503357009 | 14:90,767,611 | C/T | — | uncertain significance |
| rs201684478 | 14:90,767,623 | A/G | — | uncertain significance |
| rs8020828 | 14:90,768,183 | C/T | — | uncertain significance |
| rs1305826374 | 14:90,769,073 | C/A | — | uncertain significance |
| rs1884452697 | 14:90,769,150 | C/T | — | uncertain significance |
| rs138912467 | 14:90,769,177 | G/A | — | uncertain significance |
| rs2503359721 | 14:90,769,334 | C/A | — | uncertain significance |
| rs199890497 | 14:90,769,345 | T/C | — | uncertain significance |
| rs138706639 | 14:90,770,316 | C/G | — | uncertain significance |
| rs142705027 | 14:90,770,324 | C/T | — | likely benign |
| rs766469575 | 14:90,770,335 | T/C | — | uncertain significance |
| rs143888178 | 14:90,770,476 | T/A | — | uncertain significance |
| rs139586208 | 14:90,770,487 | G/A | — | uncertain significance |
| rs201538300 | 14:90,770,544 | G/A | — | uncertain significance |
| rs1884515561 | 14:90,770,548 | G/A | — | uncertain significance |
| rs778011988 | 14:90,770,581 | C/T | — | uncertain significance |
| rs771192087 | 14:90,770,590 | T/C | — | likely benign |
| rs769899603 | 14:90,770,611 | T/C | — | uncertain significance |
| rs2503362101 | 14:90,770,623 | C/G | — | uncertain significance |
| rs764861178 | 14:90,770,650 | C/G | — | uncertain significance |
| rs756566835 | 14:90,770,688 | G/C | — | uncertain significance |
| rs2503362318 | 14:90,770,715 | T/C | — | uncertain significance |
| rs370188454 | 14:90,778,742 | C/T | — | uncertain significance |
| rs2503372803 | 14:90,778,776 | G/C | — | uncertain significance |
| rs764288867 | 14:90,782,965 | A/T | — | uncertain significance |
| rs1004837443 | 14:90,783,004 | T/C | — | likely benign |
| rs2503378636 | 14:90,783,019 | G/A | — | uncertain significance |
| rs775945289 | 14:90,783,030 | C/G | — | uncertain significance |
| rs137945038 | 14:90,784,358 | G/A | — | uncertain significance |
| rs755456266 | 14:90,784,367 | T/G | — | uncertain significance |
| rs751310455 | 14:90,784,410 | A/G | — | uncertain significance |
| rs200339488 | 14:90,784,418 | G/T | — | uncertain significance |
| rs757702798 | 14:90,798,187 | T/C | — | uncertain significance |
| rs146229623 | 14:90,798,245 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.