RFX8
regulatory factor X8
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1032134147 | 2:102,014,078 | T/G | — | uncertain significance |
| rs765492455 | 2:102,014,129 | G/C | — | uncertain significance |
| rs1285079201 | 2:102,014,141 | T/G | — | uncertain significance |
| rs1472421522 | 2:102,014,149 | C/T | — | uncertain significance |
| rs375213952 | 2:102,018,963 | C/A | — | uncertain significance |
| rs1235103095 | 2:102,019,070 | T/C | — | uncertain significance |
| rs1488138383 | 2:102,019,095 | C/A | — | uncertain significance |
| rs1306996933 | 2:102,019,205 | T/C | — | uncertain significance |
| rs749699476 | 2:102,019,209 | A/G | — | uncertain significance |
| rs757940422 | 2:102,022,458 | A/C | — | uncertain significance |
| rs2466874149 | 2:102,022,471 | G/T | — | uncertain significance |
| rs766734511 | 2:102,029,410 | C/T | — | uncertain significance |
| rs779276390 | 2:102,029,419 | G/A | — | uncertain significance |
| rs1425589331 | 2:102,029,455 | T/A | — | uncertain significance |
| rs1365210148 | 2:102,029,457 | C/G | — | likely benign |
| rs758519979 | 2:102,029,460 | T/A | — | uncertain significance |
| rs778126119 | 2:102,029,463 | T/C | — | likely benign |
| rs1021188559 | 2:102,029,517 | A/C | — | uncertain significance |
| rs12620464 | 2:102,029,646 | T/C | intron variant | — |
| rs530834394 | 2:102,031,340 | C/G | — | uncertain significance |
| rs111964641 | 2:102,034,017 | A/C | — | likely benign |
| rs2466933501 | 2:102,034,032 | C/T | — | uncertain significance |
| rs75516500 | 2:102,035,359 | G/A | — | benign |
| rs147102001 | 2:102,035,410 | G/C | — | uncertain significance |
| rs1008197422 | 2:102,035,418 | G/A | — | likely benign |
| rs780245061 | 2:102,038,190 | C/T | — | likely benign |
| rs935523503 | 2:102,038,221 | C/T | — | uncertain significance |
| rs369894843 | 2:102,038,222 | G/C | — | uncertain significance |
| rs896621403 | 2:102,038,237 | C/T | — | uncertain significance |
| rs775822262 | 2:102,038,239 | T/C | — | uncertain significance |
| rs374167633 | 2:102,038,875 | C/A | — | uncertain significance |
| rs6744377 | 2:102,069,748 | T/A | intron variant | — |
| rs183254040 | 2:102,083,254 | C/G | — | likely benign |
| rs1344053883 | 2:102,083,264 | T/G | — | uncertain significance |
| rs564114502 | 2:102,083,273 | G/C | — | uncertain significance |
| rs371383581 | 2:102,083,295 | C/T | — | likely benign |
| rs2056067 | 2:102,085,572 | G/T | — | — |
| rs181337680 | 2:102,086,789 | G/A | intron variant | — |
| rs375793949 | 2:102,091,009 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.