ZNF44
zinc finger protein 44
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2438577 | 19:12,369,499 | G/A | upstream gene variant | — |
| rs776207200 | 19:12,383,361 | C/A | — | uncertain significance |
| rs764588639 | 19:12,383,391 | T/C | — | uncertain significance |
| rs527950258 | 19:12,383,490 | G/A | — | uncertain significance |
| rs61737484 | 19:12,383,558 | A/G | — | benign |
| rs374568983 | 19:12,383,581 | T/A | — | uncertain significance |
| rs368912997 | 19:12,383,593 | G/A | — | uncertain significance |
| rs769253969 | 19:12,383,599 | A/C | — | uncertain significance |
| rs187127429 | 19:12,383,674 | G/A | — | uncertain significance |
| rs777251487 | 19:12,383,737 | C/T | — | uncertain significance |
| rs61737490 | 19:12,383,743 | G/A | — | benign |
| rs376177505 | 19:12,383,778 | C/T | — | uncertain significance |
| rs1446550052 | 19:12,383,800 | T/C | — | uncertain significance |
| rs749714507 | 19:12,383,857 | G/A | — | uncertain significance |
| rs373408667 | 19:12,383,918 | C/T | — | uncertain significance |
| rs369182280 | 19:12,383,941 | G/A | — | uncertain significance |
| rs1224971737 | 19:12,383,967 | T/C | — | uncertain significance |
| rs2512447396 | 19:12,383,991 | G/C | — | uncertain significance |
| rs200330942 | 19:12,384,047 | T/C | — | uncertain significance |
| rs1967048248 | 19:12,384,068 | A/C | — | uncertain significance |
| rs753211268 | 19:12,384,147 | G/T | — | uncertain significance |
| rs747193093 | 19:12,384,148 | G/T | — | uncertain significance |
| rs770568540 | 19:12,384,187 | A/C | — | uncertain significance |
| rs61737486 | 19:12,384,269 | T/C | — | benign |
| rs200239042 | 19:12,384,288 | G/C | — | uncertain significance |
| rs375147934 | 19:12,384,384 | T/C | — | uncertain significance |
| rs142288021 | 19:12,384,411 | G/A | — | likely benign |
| rs150900225 | 19:12,384,432 | C/T | — | uncertain significance |
| rs549358897 | 19:12,384,433 | G/A | — | uncertain significance |
| rs2512450707 | 19:12,384,447 | C/G | — | uncertain significance |
| rs768405508 | 19:12,384,450 | A/G | — | uncertain significance |
| rs758431512 | 19:12,384,529 | G/C | — | uncertain significance |
| rs376515334 | 19:12,384,589 | T/C | — | uncertain significance |
| rs933824168 | 19:12,384,676 | C/T | — | uncertain significance |
| rs375563625 | 19:12,384,781 | G/T | — | uncertain significance |
| rs200993872 | 19:12,384,810 | A/G | — | uncertain significance |
| rs1967102933 | 19:12,384,812 | C/G | — | uncertain significance |
| rs1967149883 | 19:12,385,811 | G/T | — | uncertain significance |
| rs137984148 | 19:12,386,800 | C/G | — | likely benign |
| rs2512461724 | 19:12,386,884 | A/G | — | uncertain significance |
| rs775111986 | 19:12,404,064 | C/T | — | uncertain significance |
| rs1241986304 | 19:12,404,138 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.