ZNF155
zinc finger protein 155
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 Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs756417379 | 19:44,492,700 | C/T | — | uncertain significance |
| rs397964 | 19:44,493,969 | A/T | intron variant | — |
| rs781448076 | 19:44,496,000 | A/G | — | uncertain significance |
| rs2514256983 | 19:44,496,078 | G/A | — | uncertain significance |
| rs8104126 | 19:44,497,567 | T/C | downstream gene variant | — |
| rs78023654 | 19:44,498,950 | T/C | downstream gene variant | — |
| rs938083918 | 19:44,500,283 | G/A | — | uncertain significance |
| rs2514267895 | 19:44,500,404 | C/T | — | uncertain significance |
| rs776526186 | 19:44,500,410 | T/C | — | uncertain significance |
| rs2514268179 | 19:44,500,464 | A/G | — | uncertain significance |
| rs573263968 | 19:44,500,607 | G/A | — | uncertain significance |
| rs748630581 | 19:44,500,643 | G/A | — | uncertain significance |
| rs201225467 | 19:44,500,686 | A/G | — | uncertain significance |
| rs776521222 | 19:44,500,737 | G/A | — | uncertain significance |
| rs778551821 | 19:44,500,753 | T/A | — | uncertain significance |
| rs200344313 | 19:44,500,814 | T/C | — | uncertain significance |
| rs769698956 | 19:44,500,831 | G/T | — | likely benign |
| rs1331204127 | 19:44,500,851 | T/A | — | uncertain significance |
| rs2514270564 | 19:44,500,859 | G/T | — | uncertain significance |
| rs752339077 | 19:44,500,886 | T/C | — | uncertain significance |
| rs201204983 | 19:44,500,952 | C/T | — | uncertain significance |
| rs775166719 | 19:44,501,007 | G/T | — | uncertain significance |
| rs780250348 | 19:44,501,045 | T/A | — | uncertain significance |
| rs146476510 | 19:44,501,051 | C/G | — | likely benign |
| rs765497047 | 19:44,501,114 | G/A | — | uncertain significance |
| rs550090800 | 19:44,501,205 | G/A | — | uncertain significance |
| rs1361912257 | 19:44,501,316 | G/A | — | uncertain significance |
| rs199726372 | 19:44,501,319 | A/C | — | uncertain significance |
| rs764370096 | 19:44,501,321 | G/A | — | uncertain significance |
| rs146204893 | 19:44,501,325 | C/G | — | uncertain significance |
| rs773281921 | 19:44,501,342 | T/A | — | uncertain significance |
| rs148988125 | 19:44,501,390 | T/G | — | uncertain significance |
| rs1331384855 | 19:44,501,415 | C/T | — | uncertain significance |
| rs2514274261 | 19:44,501,436 | G/A | — | uncertain significance |
| rs368565466 | 19:44,501,466 | G/A | — | uncertain significance |
| rs780475913 | 19:44,501,486 | C/T | — | likely benign |
| rs768756682 | 19:44,501,489 | G/C | — | uncertain significance |
| rs752705382 | 19:44,501,504 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.