ZNF229
zinc finger protein 229
Summary
Predicted to enable DNA binding activity and zinc ion 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 Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs147313651 | 19:44,932,495 | C/T | — | uncertain significance |
| rs749368143 | 19:44,932,498 | C/A | — | uncertain significance |
| rs1340325463 | 19:44,932,560 | C/T | — | likely benign |
| rs753089961 | 19:44,932,563 | C/T | — | uncertain significance |
| rs778421395 | 19:44,932,566 | G/A | — | uncertain significance |
| rs2513558885 | 19:44,932,573 | G/A | — | uncertain significance |
| rs779029481 | 19:44,932,584 | G/T | — | uncertain significance |
| rs746138206 | 19:44,932,585 | T/A | — | uncertain significance |
| rs200540195 | 19:44,932,609 | G/A | — | uncertain significance |
| rs375182987 | 19:44,932,704 | T/C | — | uncertain significance |
| rs373898116 | 19:44,932,777 | G/A | — | uncertain significance |
| rs370335801 | 19:44,932,858 | G/A | — | uncertain significance |
| rs758382409 | 19:44,932,866 | G/C | — | uncertain significance |
| rs200873280 | 19:44,932,899 | C/A | — | uncertain significance |
| rs754516445 | 19:44,932,920 | G/A | — | uncertain significance |
| rs1434579 | 19:44,932,972 | C/A | stop gained | — |
| rs1971638276 | 19:44,932,993 | G/A | — | uncertain significance |
| rs199930833 | 19:44,933,061 | T/G | — | uncertain significance |
| rs201858404 | 19:44,933,107 | T/C | — | uncertain significance |
| rs1435316745 | 19:44,933,118 | G/A | — | uncertain significance |
| rs372929381 | 19:44,933,155 | C/T | — | uncertain significance |
| rs377119196 | 19:44,933,170 | C/T | — | uncertain significance |
| rs1048371877 | 19:44,933,182 | T/C | — | uncertain significance |
| rs370451566 | 19:44,933,209 | G/A | — | uncertain significance |
| rs183052577 | 19:44,933,212 | G/A | — | likely benign |
| rs573525946 | 19:44,933,284 | C/T | — | uncertain significance |
| rs200189575 | 19:44,933,355 | A/G | — | likely benign |
| rs772552130 | 19:44,933,395 | C/T | — | uncertain significance |
| rs201763580 | 19:44,933,467 | C/T | — | likely benign |
| rs201533514 | 19:44,933,513 | C/A | — | likely benign |
| rs750679752 | 19:44,933,533 | G/A | — | uncertain significance |
| rs773871311 | 19:44,933,566 | C/A | — | uncertain significance |
| rs771791820 | 19:44,933,596 | T/C | — | likely benign |
| rs766637877 | 19:44,933,728 | A/G | — | uncertain significance |
| rs1172983268 | 19:44,933,803 | C/A | — | uncertain significance |
| rs367731023 | 19:44,933,871 | G/A | — | uncertain significance |
| rs201823616 | 19:44,933,895 | C/T | — | uncertain significance |
| rs199919052 | 19:44,933,901 | T/A | — | uncertain significance |
| rs756441943 | 19:44,933,906 | T/A | — | uncertain significance |
| rs771367490 | 19:44,933,910 | T/C | — | uncertain significance |
| rs2513566312 | 19:44,933,913 | G/A | — | likely benign |
| rs201536141 | 19:44,933,979 | C/T | — | uncertain significance |
| rs1555725717 | 19:44,933,990 | C/G | — | uncertain significance |
| rs759353264 | 19:44,934,055 | C/T | — | uncertain significance |
| rs759532690 | 19:44,934,115 | G/A | — | uncertain significance |
| rs374653789 | 19:44,934,126 | T/A | — | uncertain significance |
| rs1197789974 | 19:44,934,136 | A/G | — | uncertain significance |
| rs748406342 | 19:44,934,181 | T/C | — | uncertain significance |
| rs778772232 | 19:44,934,186 | C/A | — | uncertain significance |
| rs750860423 | 19:44,934,231 | C/A | — | uncertain significance |
| rs965363574 | 19:44,934,312 | C/T | — | uncertain significance |
| rs1233996530 | 19:44,934,409 | G/A | — | uncertain significance |
| rs529237934 | 19:44,934,414 | G/A | — | uncertain significance |
| rs375016098 | 19:44,934,499 | T/G | — | uncertain significance |
| rs200548188 | 19:44,934,502 | G/T | — | uncertain significance |
| rs980634203 | 19:44,934,510 | G/A | — | uncertain significance |
| rs761096293 | 19:44,934,522 | C/A | — | uncertain significance |
| rs1473222739 | 19:44,934,612 | T/A | — | uncertain significance |
| rs141153185 | 19:44,934,613 | C/T | — | uncertain significance |
| rs763168113 | 19:44,934,651 | T/C | — | uncertain significance |
| rs749884596 | 19:44,934,687 | A/T | — | uncertain significance |
| rs2513573885 | 19:44,936,431 | C/G | — | uncertain significance |
| rs367712470 | 19:44,936,520 | C/T | — | uncertain significance |
| rs144627165 | 19:44,946,195 | G/A | intron variant | — |
| rs199644935 | 19:44,947,030 | A/G | — | likely benign |
| rs2722698 | 19:44,950,550 | G/A | intron variant | — |
| rs926052 | 19:44,952,236 | A/C | — | — |
| rs143783837 | 19:44,952,606 | C/T | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.