ZNF226
zinc finger protein 226
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 Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs771432384 | 19:44,674,238 | A/G | — | likely benign |
| rs752607335 | 19:44,676,262 | G/A | — | uncertain significance |
| rs371884663 | 19:44,676,266 | C/T | — | uncertain significance |
| rs1388121224 | 19:44,676,299 | T/C | — | uncertain significance |
| rs199602003 | 19:44,676,340 | G/A | — | uncertain significance |
| rs769103178 | 19:44,676,365 | T/C | — | uncertain significance |
| rs1256946134 | 19:44,677,021 | C/G | — | uncertain significance |
| rs1555783337 | 19:44,677,027 | A/C | — | uncertain significance |
| rs200875397 | 19:44,677,061 | A/G | — | likely benign |
| rs371422117 | 19:44,677,076 | C/T | — | uncertain significance |
| rs1055399709 | 19:44,679,740 | A/G | — | uncertain significance |
| rs780148352 | 19:44,679,864 | T/G | — | uncertain significance |
| rs769401601 | 19:44,679,885 | A/G | — | likely benign |
| rs1031912005 | 19:44,679,968 | A/G | — | uncertain significance |
| rs374027023 | 19:44,680,004 | T/C | — | uncertain significance |
| rs1262798925 | 19:44,680,028 | C/G | — | uncertain significance |
| rs551109276 | 19:44,680,031 | A/C | — | uncertain significance |
| rs371556470 | 19:44,680,095 | A/T | — | uncertain significance |
| rs188862419 | 19:44,680,115 | A/G | — | uncertain significance |
| rs775862847 | 19:44,680,121 | A/T | — | uncertain significance |
| rs759409614 | 19:44,680,151 | C/T | — | uncertain significance |
| rs778546246 | 19:44,680,167 | C/T | — | uncertain significance |
| rs199908530 | 19:44,680,242 | G/A | — | uncertain significance |
| rs1461750949 | 19:44,680,284 | G/A | — | uncertain significance |
| rs751106639 | 19:44,680,367 | C/A | — | uncertain significance |
| rs1446862630 | 19:44,680,512 | A/T | — | uncertain significance |
| rs764509648 | 19:44,680,516 | G/C | — | uncertain significance |
| rs540717109 | 19:44,680,590 | A/G | — | uncertain significance |
| rs1206197925 | 19:44,680,596 | A/T | — | uncertain significance |
| rs771640806 | 19:44,680,620 | G/A | — | uncertain significance |
| rs765679534 | 19:44,680,667 | C/T | — | uncertain significance |
| rs755235933 | 19:44,680,682 | G/A | — | uncertain significance |
| rs766842293 | 19:44,680,797 | G/A | — | uncertain significance |
| rs759539042 | 19:44,680,860 | A/C | — | uncertain significance |
| rs769558345 | 19:44,680,907 | A/G | — | uncertain significance |
| rs372362519 | 19:44,680,932 | A/G | — | likely benign |
| rs2514649197 | 19:44,680,992 | C/T | — | uncertain significance |
| rs2514649665 | 19:44,681,025 | G/A | — | uncertain significance |
| rs981577820 | 19:44,681,115 | G/A | — | uncertain significance |
| rs536017980 | 19:44,681,160 | C/G | — | uncertain significance |
| rs2514652060 | 19:44,681,201 | T/G | — | uncertain significance |
| rs575965116 | 19:44,681,208 | G/A | — | uncertain significance |
| rs1442943935 | 19:44,681,222 | A/C | — | uncertain significance |
| rs370984107 | 19:44,681,227 | T/G | — | uncertain significance |
| rs370723092 | 19:44,681,262 | A/T | — | uncertain significance |
| rs2514652927 | 19:44,681,272 | G/C | — | uncertain significance |
| rs558229787 | 19:44,681,282 | G/A | — | uncertain significance |
| rs762065164 | 19:44,681,475 | A/T | — | uncertain significance |
| rs375854040 | 19:44,681,568 | A/G | — | uncertain significance |
| rs2514657519 | 19:44,681,591 | C/T | — | uncertain significance |
| rs370753005 | 19:44,681,597 | A/C | — | uncertain significance |
| rs766519729 | 19:44,681,655 | G/A | — | uncertain significance |
| rs778990236 | 19:44,681,693 | T/C | — | uncertain significance |
| rs1970818934 | 19:44,681,745 | A/G | — | uncertain significance |
| rs1240436478 | 19:44,681,772 | A/G | — | uncertain significance |
| rs980938320 | 19:44,681,785 | G/C | — | uncertain significance |
| rs2514661252 | 19:44,681,807 | G/A | — | uncertain significance |
| rs142963756 | 19:44,683,169 | C/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.