NR2F6
nuclear receptor subfamily 2 group F member 6
Summary
Enables DNA-binding transcription factor activity and sequence-specific double-stranded DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs746238290 | 19:17,343,171 | G/A | — | uncertain significance |
| rs370347405 | 19:17,343,175 | C/T | — | uncertain significance |
| rs1308630585 | 19:17,343,196 | T/C | — | uncertain significance |
| rs1228309806 | 19:17,343,291 | G/A | — | uncertain significance |
| rs139615269 | 19:17,343,292 | C/T | — | uncertain significance |
| rs1408723803 | 19:17,343,375 | G/A | — | uncertain significance |
| rs2513043374 | 19:17,343,379 | C/T | — | uncertain significance |
| rs1358563233 | 19:17,346,344 | A/T | — | uncertain significance |
| rs2513045682 | 19:17,346,361 | T/C | — | uncertain significance |
| rs765880765 | 19:17,346,404 | C/A | — | uncertain significance |
| rs1159678089 | 19:17,346,448 | G/C | — | uncertain significance |
| rs746051796 | 19:17,346,463 | G/A | — | uncertain significance |
| rs1244300442 | 19:17,346,481 | G/A | — | uncertain significance |
| rs1468040326 | 19:17,346,508 | G/A | — | uncertain significance |
| rs1275857402 | 19:17,346,653 | T/C | — | uncertain significance |
| rs1163044697 | 19:17,346,715 | G/A | — | uncertain significance |
| rs2513046354 | 19:17,346,770 | G/A | — | uncertain significance |
| rs973007907 | 19:17,346,794 | C/T | — | uncertain significance |
| rs1399134499 | 19:17,346,805 | C/G | — | uncertain significance |
| rs1014830725 | 19:17,346,820 | G/A | — | uncertain significance |
| rs764556511 | 19:17,346,853 | G/A | — | uncertain significance |
| rs202200760 | 19:17,346,854 | G/C | missense variant | — |
| rs1030004933 | 19:17,346,857 | T/C | — | uncertain significance |
| rs2513046578 | 19:17,346,863 | C/T | — | uncertain significance |
| rs146541423 | 19:17,351,501 | G/A | — | uncertain significance |
| rs4808611 | 19:17,354,825 | C/A | — | — |
| rs771214764 | 19:17,355,940 | G/T | — | likely benign |
| rs769815988 | 19:17,355,978 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.