ZNF343
zinc finger protein 343
Summary
Enables sequence-specific double-stranded 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 Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759046941 | 20:2,463,843 | A/C | — | uncertain significance |
| rs556099913 | 20:2,463,860 | C/T | — | uncertain significance |
| rs896564332 | 20:2,463,863 | A/G | — | uncertain significance |
| rs372354666 | 20:2,463,901 | C/T | — | uncertain significance |
| rs535851423 | 20:2,463,928 | C/T | — | likely benign |
| rs146638299 | 20:2,463,929 | G/A | — | uncertain significance |
| rs554431460 | 20:2,463,930 | G/A | — | likely benign |
| rs757699168 | 20:2,463,935 | A/C | — | uncertain significance |
| rs746885025 | 20:2,463,960 | G/A | — | likely benign |
| rs151238644 | 20:2,463,975 | T/A | — | likely benign |
| rs140436866 | 20:2,463,981 | T/C | — | likely benign |
| rs769462325 | 20:2,463,986 | T/G | — | likely benign |
| rs774918301 | 20:2,463,990 | A/G | — | likely benign |
| rs763443890 | 20:2,463,996 | A/G | — | likely benign |
| rs369112935 | 20:2,464,018 | A/G | — | uncertain significance |
| rs749633550 | 20:2,464,114 | C/T | — | uncertain significance |
| rs374101325 | 20:2,464,180 | C/T | — | uncertain significance |
| rs528685225 | 20:2,464,182 | A/G | — | likely benign |
| rs144403061 | 20:2,464,183 | C/T | — | uncertain significance |
| rs746493659 | 20:2,464,206 | A/G | — | likely benign |
| rs149860498 | 20:2,464,217 | G/T | — | uncertain significance |
| rs146214742 | 20:2,464,234 | G/A | — | likely benign |
| rs755245255 | 20:2,464,241 | C/G | — | uncertain significance |
| rs142385929 | 20:2,464,301 | G/T | — | uncertain significance |
| rs372746408 | 20:2,464,445 | G/C | — | uncertain significance |
| rs947626394 | 20:2,464,468 | G/C | — | uncertain significance |
| rs748234345 | 20:2,464,744 | T/A | — | uncertain significance |
| rs201630435 | 20:2,464,760 | T/C | — | likely benign |
| rs757063219 | 20:2,464,789 | T/C | — | uncertain significance |
| rs1183080545 | 20:2,464,804 | G/A | — | uncertain significance |
| rs148685627 | 20:2,464,915 | T/C | — | uncertain significance |
| rs777830124 | 20:2,464,921 | C/G | — | uncertain significance |
| rs750583060 | 20:2,465,162 | C/T | — | likely benign |
| rs754222312 | 20:2,465,201 | A/G | — | uncertain significance |
| rs2514462613 | 20:2,465,214 | G/C | — | uncertain significance |
| rs539865734 | 20:2,465,227 | T/C | — | uncertain significance |
| rs773144691 | 20:2,465,261 | G/C | — | uncertain significance |
| rs2514507764 | 20:2,474,197 | G/C | — | uncertain significance |
| rs892372281 | 20:2,474,494 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.