NWD2
NACHT and WD repeat domain containing 2
Summary
Predicted to be active in synapse. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants83 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1374191923 | 4:37,246,706 | C/T | — | uncertain significance |
| rs1048096970 | 4:37,246,784 | C/T | — | uncertain significance |
| rs1203792953 | 4:37,246,816 | G/A | — | uncertain significance |
| rs905839831 | 4:37,259,551 | T/C | — | — |
| rs867133582 | 4:37,358,052 | G/A | — | uncertain significance |
| rs749493492 | 4:37,358,069 | A/C | — | uncertain significance |
| rs774664515 | 4:37,358,087 | G/T | — | uncertain significance |
| rs2474977136 | 4:37,358,097 | G/C | — | uncertain significance |
| rs28582192 | 4:37,388,087 | C/T | intron variant | — |
| rs973494027 | 4:37,432,227 | A/G | — | uncertain significance |
| rs1201134593 | 4:37,432,269 | G/A | — | uncertain significance |
| rs759392547 | 4:37,432,275 | G/A | — | uncertain significance |
| rs769997174 | 4:37,432,276 | C/T | — | uncertain significance |
| rs184375612 | 4:37,432,292 | G/A | — | likely benign |
| rs1167737230 | 4:37,432,300 | A/C | — | uncertain significance |
| rs2475046687 | 4:37,432,360 | G/C | — | uncertain significance |
| rs148102451 | 4:37,432,376 | G/A | — | uncertain significance |
| rs750902582 | 4:37,432,391 | A/C | — | uncertain significance |
| rs1226341541 | 4:37,435,511 | C/T | — | uncertain significance |
| rs183200253 | 4:37,435,593 | C/T | — | likely benign |
| rs2475049748 | 4:37,435,631 | A/T | — | uncertain significance |
| rs189191557 | 4:37,440,516 | A/G | — | uncertain significance |
| rs1424864224 | 4:37,440,585 | G/A | — | uncertain significance |
| rs892491181 | 4:37,440,596 | G/A | — | uncertain significance |
| rs780123645 | 4:37,440,600 | A/T | — | uncertain significance |
| rs2475054563 | 4:37,440,807 | C/G | — | uncertain significance |
| rs2475054608 | 4:37,440,843 | A/G | — | uncertain significance |
| rs570036994 | 4:37,440,861 | C/T | — | uncertain significance |
| rs182008355 | 4:37,440,866 | G/A | — | uncertain significance |
| rs200042443 | 4:37,440,896 | C/A | — | uncertain significance |
| rs142523381 | 4:37,445,144 | A/G | — | benign |
| rs376203240 | 4:37,445,210 | C/T | — | uncertain significance |
| rs2475058829 | 4:37,445,231 | A/T | — | uncertain significance |
| rs1251446347 | 4:37,445,254 | C/G | — | uncertain significance |
| rs892139373 | 4:37,445,286 | T/C | — | uncertain significance |
| rs1712547213 | 4:37,445,288 | A/T | — | uncertain significance |
| rs2475059487 | 4:37,445,439 | C/T | — | uncertain significance |
| rs750624693 | 4:37,445,490 | A/G | — | uncertain significance |
| rs754793058 | 4:37,445,495 | G/A | — | uncertain significance |
| rs73133791 | 4:37,445,521 | C/T | — | likely benign |
| rs373564222 | 4:37,445,528 | G/A | — | uncertain significance |
| rs370059705 | 4:37,445,529 | A/G | — | uncertain significance |
| rs370627496 | 4:37,445,624 | C/G | — | uncertain significance |
| rs141630665 | 4:37,445,727 | T/C | — | uncertain significance |
| rs181518983 | 4:37,445,751 | G/A | — | uncertain significance |
| rs1215122172 | 4:37,445,784 | A/G | — | uncertain significance |
| rs981570586 | 4:37,445,793 | C/T | — | uncertain significance |
| rs2475060429 | 4:37,446,065 | T/C | — | uncertain significance |
| rs1043628238 | 4:37,446,095 | G/A | — | uncertain significance |
| rs2475060558 | 4:37,446,165 | A/G | — | uncertain significance |
| rs954049070 | 4:37,446,308 | A/C | — | uncertain significance |
| rs764641204 | 4:37,446,385 | G/A | — | likely benign |
| rs201434818 | 4:37,446,452 | C/T | — | likely benign |
| rs200234605 | 4:37,446,489 | G/A | — | uncertain significance |
| rs779464479 | 4:37,446,517 | T/A | — | uncertain significance |
| rs370757218 | 4:37,446,601 | G/C | — | uncertain significance |
| rs1272500365 | 4:37,446,735 | G/T | — | uncertain significance |
| rs2475061330 | 4:37,446,754 | A/C | — | uncertain significance |
| rs145389202 | 4:37,446,781 | C/A | — | uncertain significance |
| rs765006404 | 4:37,446,821 | G/A | — | uncertain significance |
| rs115501832 | 4:37,446,829 | A/T | — | benign |
| rs375871515 | 4:37,446,882 | C/T | — | uncertain significance |
| rs2475061490 | 4:37,446,897 | A/C | — | uncertain significance |
| rs370813973 | 4:37,447,035 | G/A | — | uncertain significance |
| rs374145065 | 4:37,447,186 | G/T | — | likely benign |
| rs2475062260 | 4:37,447,263 | G/T | — | uncertain significance |
| rs569100480 | 4:37,447,308 | G/A | — | uncertain significance |
| rs771733784 | 4:37,447,359 | T/G | — | uncertain significance |
| rs2475062718 | 4:37,447,584 | C/T | — | uncertain significance |
| rs758352844 | 4:37,447,601 | A/G | — | uncertain significance |
| rs187072975 | 4:37,447,798 | C/T | — | likely benign |
| rs901369475 | 4:37,447,806 | G/A | — | uncertain significance |
| rs904530364 | 4:37,447,976 | A/G | — | uncertain significance |
| rs770904759 | 4:37,448,042 | G/A | — | uncertain significance |
| rs567881077 | 4:37,448,093 | G/A | — | uncertain significance |
| rs73133793 | 4:37,448,107 | G/A | — | likely benign |
| rs557580112 | 4:37,448,189 | C/A | — | uncertain significance |
| rs2475063975 | 4:37,448,231 | A/G | — | uncertain significance |
| rs200088519 | 4:37,448,297 | G/A | — | uncertain significance |
| rs777752418 | 4:37,448,533 | G/C | — | likely benign |
| rs150379960 | 4:37,448,552 | C/T | — | uncertain significance |
| rs1415236230 | 4:37,448,663 | T/C | — | uncertain significance |
| rs1712658791 | 4:37,448,723 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.