ZNF285
zinc finger protein 285
Summary
Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4142248 | 19:44,888,276 | T/C | intron variant | — |
| rs749334484 | 19:44,890,656 | T/C | — | uncertain significance |
| rs2513526073 | 19:44,890,677 | A/G | — | uncertain significance |
| rs73039936 | 19:44,890,685 | T/C | — | likely benign |
| rs148896964 | 19:44,890,825 | T/C | — | uncertain significance |
| rs143574007 | 19:44,890,887 | A/G | — | likely benign |
| rs568314396 | 19:44,890,944 | A/C | — | uncertain significance |
| rs773590565 | 19:44,890,948 | C/T | — | uncertain significance |
| rs141226346 | 19:44,890,969 | C/G | missense variant | — |
| rs2513526777 | 19:44,890,974 | T/G | — | uncertain significance |
| rs562822636 | 19:44,891,116 | C/T | — | uncertain significance |
| rs1301046424 | 19:44,891,143 | G/C | — | uncertain significance |
| rs766969013 | 19:44,891,181 | A/C | — | uncertain significance |
| rs1971094469 | 19:44,891,211 | G/A | — | uncertain significance |
| rs535569015 | 19:44,891,218 | C/T | — | uncertain significance |
| rs774912290 | 19:44,891,258 | C/G | — | uncertain significance |
| rs753470924 | 19:44,891,268 | C/G | — | uncertain significance |
| rs372504763 | 19:44,891,274 | C/G | — | uncertain significance |
| rs2513527613 | 19:44,891,331 | A/G | — | uncertain significance |
| rs145215668 | 19:44,891,364 | T/A | — | likely benign |
| rs1364201580 | 19:44,891,365 | C/T | — | uncertain significance |
| rs202025427 | 19:44,891,368 | C/T | — | likely benign |
| rs2513527712 | 19:44,891,376 | T/C | — | uncertain significance |
| rs201861898 | 19:44,891,401 | G/C | — | uncertain significance |
| rs151191161 | 19:44,891,423 | G/C | — | uncertain significance |
| rs772929619 | 19:44,891,424 | C/T | — | likely benign |
| rs774827964 | 19:44,891,503 | C/A | — | uncertain significance |
| rs1183075800 | 19:44,891,527 | G/A | — | uncertain significance |
| rs1372696154 | 19:44,891,663 | A/C | — | uncertain significance |
| rs776001232 | 19:44,891,689 | C/G | — | uncertain significance |
| rs373787402 | 19:44,891,710 | G/T | — | likely benign |
| rs551385384 | 19:44,891,779 | C/T | — | uncertain significance |
| rs902316370 | 19:44,891,828 | A/T | — | uncertain significance |
| rs376769237 | 19:44,891,881 | A/C | — | uncertain significance |
| rs368793630 | 19:44,891,890 | C/T | — | uncertain significance |
| rs750298852 | 19:44,891,992 | G/T | — | likely benign |
| rs2123264042 | 19:44,892,002 | G/C | — | uncertain significance |
| rs753070130 | 19:44,892,006 | T/C | — | uncertain significance |
| rs143200727 | 19:44,892,106 | G/T | — | uncertain significance |
| rs2513529537 | 19:44,892,115 | A/C | — | uncertain significance |
| rs572775397 | 19:44,892,177 | C/G | — | uncertain significance |
| rs117953191 | 19:44,892,228 | G/T | — | likely benign |
| rs113465092 | 19:44,896,564 | C/A | — | likely benign |
| rs749677045 | 19:44,896,597 | A/G | — | uncertain significance |
| rs145494710 | 19:44,903,050 | T/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.