ADNP2
ADNP homeobox 2
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Predicted to be involved in nervous system development and regulation of gene expression. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants72 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2512163322 | 18:77,875,489 | A/G | — | uncertain significance |
| rs766615425 | 18:77,875,514 | G/A | — | uncertain significance |
| rs2052509354 | 18:77,891,032 | C/T | — | uncertain significance |
| rs199819195 | 18:77,891,038 | G/T | — | uncertain significance |
| rs1323425831 | 18:77,891,043 | G/A | — | likely benign |
| rs867194748 | 18:77,891,062 | C/A | — | uncertain significance |
| rs1437152279 | 18:77,893,549 | C/T | — | uncertain significance |
| rs561449125 | 18:77,893,565 | A/T | — | uncertain significance |
| rs772830301 | 18:77,893,574 | A/G | — | uncertain significance |
| rs1369315320 | 18:77,893,577 | G/A | — | uncertain significance |
| rs2052527503 | 18:77,893,587 | A/T | — | uncertain significance |
| rs779099751 | 18:77,893,685 | C/G | — | uncertain significance |
| rs771842203 | 18:77,893,690 | C/T | — | uncertain significance |
| rs564833550 | 18:77,893,706 | A/G | — | uncertain significance |
| rs371521990 | 18:77,893,880 | G/A | — | likely benign |
| rs368516384 | 18:77,893,900 | G/A | — | uncertain significance |
| rs745873475 | 18:77,893,921 | A/G | — | uncertain significance |
| rs2512180387 | 18:77,893,922 | T/C | — | uncertain significance |
| rs141268043 | 18:77,893,964 | A/G | — | uncertain significance |
| rs142109614 | 18:77,894,087 | C/T | — | likely benign |
| rs540505059 | 18:77,894,155 | G/A | — | uncertain significance |
| rs571198421 | 18:77,894,266 | C/T | — | uncertain significance |
| rs1365581197 | 18:77,894,272 | G/C | — | uncertain significance |
| rs749973024 | 18:77,894,287 | A/G | — | likely benign |
| rs201074994 | 18:77,894,374 | G/A | — | uncertain significance |
| rs976294689 | 18:77,894,400 | T/A | — | uncertain significance |
| rs139283796 | 18:77,894,424 | G/T | — | uncertain significance |
| rs766046056 | 18:77,894,575 | C/T | — | uncertain significance |
| rs376361164 | 18:77,894,630 | C/T | — | uncertain significance |
| rs1394106687 | 18:77,894,648 | C/G | — | uncertain significance |
| rs141068587 | 18:77,894,698 | G/A | — | uncertain significance |
| rs370054347 | 18:77,894,725 | C/T | — | uncertain significance |
| rs745663476 | 18:77,894,777 | C/T | — | uncertain significance |
| rs370507445 | 18:77,894,884 | G/C | — | uncertain significance |
| rs2512183183 | 18:77,894,992 | C/A | — | uncertain significance |
| rs776698719 | 18:77,895,187 | C/T | — | uncertain significance |
| rs755507497 | 18:77,895,203 | C/A | — | uncertain significance |
| rs572333470 | 18:77,895,268 | G/A | — | likely benign |
| rs2512183963 | 18:77,895,346 | A/C | — | uncertain significance |
| rs35954328 | 18:77,895,408 | G/A | — | likely benign |
| rs892223872 | 18:77,895,413 | A/G | — | uncertain significance |
| rs750640679 | 18:77,895,493 | G/T | — | uncertain significance |
| rs2512184346 | 18:77,895,527 | A/G | — | uncertain significance |
| rs1217048281 | 18:77,895,697 | A/G | — | likely benign |
| rs1259142788 | 18:77,895,806 | G/A | — | uncertain significance |
| rs141108203 | 18:77,895,823 | A/G | — | uncertain significance |
| rs750244801 | 18:77,895,902 | G/A | — | uncertain significance |
| rs746248622 | 18:77,895,944 | C/T | — | uncertain significance |
| rs374200956 | 18:77,896,092 | C/T | — | likely benign |
| rs368537313 | 18:77,896,093 | G/A | — | likely benign |
| rs1474057296 | 18:77,896,105 | C/T | — | uncertain significance |
| rs760732249 | 18:77,896,123 | A/G | — | uncertain significance |
| rs561195907 | 18:77,896,131 | C/G | — | uncertain significance |
| rs2512185601 | 18:77,896,153 | C/T | — | uncertain significance |
| rs2512185656 | 18:77,896,180 | C/T | — | uncertain significance |
| rs1401599031 | 18:77,896,243 | G/A | — | uncertain significance |
| rs1175925435 | 18:77,896,247 | A/G | — | uncertain significance |
| rs771009049 | 18:77,896,258 | G/A | — | uncertain significance |
| rs1377955375 | 18:77,896,274 | G/A | — | uncertain significance |
| rs2052557784 | 18:77,896,285 | C/T | — | uncertain significance |
| rs755347851 | 18:77,896,303 | G/C | — | uncertain significance |
| rs956866568 | 18:77,896,304 | A/G | — | uncertain significance |
| rs148260789 | 18:77,896,318 | C/G | — | uncertain significance |
| rs141359018 | 18:77,896,331 | C/T | — | uncertain significance |
| rs2052558642 | 18:77,896,362 | T/A | — | uncertain significance |
| rs1365693619 | 18:77,896,384 | A/G | — | uncertain significance |
| rs2512186225 | 18:77,896,420 | G/C | — | uncertain significance |
| rs200163506 | 18:77,896,427 | A/G | — | uncertain significance |
| rs145603867 | 18:77,896,442 | G/A | — | uncertain significance |
| rs376709771 | 18:77,896,529 | C/T | — | uncertain significance |
| rs778709997 | 18:77,896,535 | T/C | — | uncertain significance |
| rs767845192 | 18:77,896,619 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.