ZNF526
zinc finger protein 526
Summary
Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1021674497 | 19:42,728,554 | C/T | — | uncertain significance |
| rs1394553795 | 19:42,728,602 | C/G | — | uncertain significance |
| rs149913848 | 19:42,728,636 | G/A | — | conflicting classifications of pathogenicity |
| rs146838645 | 19:42,728,658 | A/G | — | uncertain significance |
| rs3810151 | 19:42,728,836 | T/C | — | benign |
| rs2513490533 | 19:42,728,844 | G/C | — | uncertain significance |
| rs772605156 | 19:42,728,859 | C/G | — | uncertain significance |
| rs529515334 | 19:42,728,896 | G/A | — | uncertain significance |
| rs146635897 | 19:42,728,950 | G/A | — | uncertain significance |
| rs730882205 | 19:42,729,034 | A/C | missense variant | pathogenic |
| rs57984044 | 19:42,729,056 | G/A | — | benign |
| rs143231579 | 19:42,729,069 | C/A | — | uncertain significance |
| rs150807158 | 19:42,729,121 | C/T | — | benign |
| rs767991329 | 19:42,729,174 | G/A | — | uncertain significance |
| rs569291252 | 19:42,729,311 | G/A | — | uncertain significance |
| rs147068650 | 19:42,729,327 | G/A | — | uncertain significance |
| rs377045934 | 19:42,729,351 | G/A | — | uncertain significance |
| rs138082392 | 19:42,729,380 | C/T | — | conflicting classifications of pathogenicity |
| rs370031955 | 19:42,729,381 | G/A | — | uncertain significance |
| rs551317806 | 19:42,729,408 | G/T | — | uncertain significance |
| rs764720592 | 19:42,729,417 | C/T | — | uncertain significance |
| rs768788891 | 19:42,729,424 | A/C | — | uncertain significance |
| rs954678772 | 19:42,729,465 | C/T | — | uncertain significance |
| rs780428240 | 19:42,729,489 | C/T | — | uncertain significance |
| rs747300825 | 19:42,729,493 | G/A | — | uncertain significance |
| rs138927181 | 19:42,729,510 | C/T | — | uncertain significance |
| rs773722181 | 19:42,729,511 | G/A | — | uncertain significance |
| rs1207022095 | 19:42,729,549 | C/T | — | likely benign |
| rs144433879 | 19:42,729,610 | G/A | — | conflicting classifications of pathogenicity |
| rs1201644078 | 19:42,729,782 | C/G | — | pathogenic |
| rs370257568 | 19:42,729,786 | G/A | — | uncertain significance |
| rs144394848 | 19:42,729,835 | C/T | — | uncertain significance |
| rs764270261 | 19:42,729,844 | C/G | — | uncertain significance |
| rs2036171317 | 19:42,729,886 | G/T | — | uncertain significance |
| rs146618152 | 19:42,729,922 | G/A | — | uncertain significance |
| rs759579625 | 19:42,729,936 | C/T | — | uncertain significance |
| rs760348469 | 19:42,729,939 | C/T | — | uncertain significance |
| rs368283243 | 19:42,729,964 | G/A | — | uncertain significance |
| rs776395707 | 19:42,730,011 | C/T | — | uncertain significance |
| rs145696319 | 19:42,730,013 | C/T | — | likely benign |
| rs369862002 | 19:42,730,040 | G/A | — | uncertain significance |
| rs370533115 | 19:42,730,079 | C/A | — | likely benign |
| rs780047979 | 19:42,730,099 | T/G | — | uncertain significance |
| rs2513492986 | 19:42,730,138 | A/G | — | uncertain significance |
| rs587780525 | 19:42,730,140 | C/T | — | benign |
| rs147052277 | 19:42,730,161 | C/T | — | uncertain significance |
| rs200943083 | 19:42,730,162 | G/T | — | uncertain significance |
| rs2513493061 | 19:42,730,183 | T/C | — | uncertain significance |
| rs587780523 | 19:42,730,204 | A/C | — | benign |
| rs111722832 | 19:42,730,217 | C/T | — | benign |
| rs148255924 | 19:42,730,223 | T/A | — | likely benign |
| rs776086354 | 19:42,730,227 | C/T | — | uncertain significance |
| rs200018551 | 19:42,730,230 | G/A | — | conflicting classifications of pathogenicity |
| rs749529712 | 19:42,730,313 | G/A | — | uncertain significance |
| rs765960978 | 19:42,730,332 | C/T | — | uncertain significance |
| rs775749276 | 19:42,730,366 | A/G | — | uncertain significance |
| rs370949355 | 19:42,730,386 | C/T | — | uncertain significance |
| rs200931477 | 19:42,730,399 | C/T | — | uncertain significance |
| rs797046129 | 19:42,730,425 | A/G | — | uncertain significance |
| rs1218926426 | 19:42,730,449 | A/G | — | uncertain significance |
| rs143303371 | 19:42,730,536 | G/A | — | uncertain significance |
| rs971401936 | 19:42,730,555 | C/T | — | uncertain significance |
| rs758206052 | 19:42,730,557 | G/C | — | uncertain significance |
| rs755140702 | 19:42,730,569 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.