CARF
calcium responsive transcription factor
Summary
Enables DNA binding activity and DNA-binding transcription activator activity, RNA polymerase II-specific. Involved in cellular response to calcium ion. Predicted to be located in granular component. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7603972 | 2:203,780,515 | A/G | upstream gene variant | — |
| rs114393235 | 2:203,795,987 | T/C | — | — |
| rs72926767 | 2:203,796,814 | C/G | intron variant | — |
| rs72926770 | 2:203,798,585 | C/T | — | — |
| rs72926772 | 2:203,804,289 | C/T | intron variant | — |
| rs2058247206 | 2:203,806,657 | A/C | — | uncertain significance |
| rs149943854 | 2:203,806,666 | A/G | — | uncertain significance |
| rs1250963666 | 2:203,807,488 | A/T | — | uncertain significance |
| rs745904615 | 2:203,807,538 | C/T | — | uncertain significance |
| rs765919935 | 2:203,807,581 | C/T | — | uncertain significance |
| rs2058302212 | 2:203,807,652 | T/C | — | uncertain significance |
| rs115268453 | 2:203,817,297 | C/T | — | likely benign |
| rs2469023714 | 2:203,817,318 | C/A | — | uncertain significance |
| rs1417720726 | 2:203,817,349 | T/A | — | uncertain significance |
| rs1375561549 | 2:203,817,354 | C/G | — | uncertain significance |
| rs899016056 | 2:203,817,370 | A/G | — | uncertain significance |
| rs758931336 | 2:203,817,399 | C/T | — | uncertain significance |
| rs372978113 | 2:203,818,766 | A/G | — | uncertain significance |
| rs35438756 | 2:203,818,770 | T/C | — | likely benign |
| rs2469037054 | 2:203,818,775 | G/A | — | uncertain significance |
| rs2469037879 | 2:203,818,833 | C/T | — | uncertain significance |
| rs201808511 | 2:203,818,856 | G/A | — | likely benign |
| rs116678869 | 2:203,819,471 | A/G | intron variant | — |
| rs3731695 | 2:203,820,275 | T/C | intron variant | — |
| rs2469052531 | 2:203,820,455 | T/A | — | uncertain significance |
| rs539997380 | 2:203,825,502 | T/C | — | — |
| rs200793099 | 2:203,826,045 | G/A | — | uncertain significance |
| rs375805618 | 2:203,826,089 | A/G | — | uncertain significance |
| rs114123510 | 2:203,831,212 | T/A | intron variant | — |
| rs72928605 | 2:203,832,120 | A/G | intron variant | — |
| rs73056727 | 2:203,834,636 | A/T | — | benign |
| rs1239962536 | 2:203,834,646 | T/C | — | uncertain significance |
| rs749820336 | 2:203,834,763 | G/A | — | uncertain significance |
| rs202084612 | 2:203,836,284 | C/G | — | uncertain significance |
| rs1334453319 | 2:203,836,440 | A/C | — | uncertain significance |
| rs78815956 | 2:203,839,087 | C/T | — | benign |
| rs6721180 | 2:203,842,015 | G/A | — | benign |
| rs72932557 | 2:203,846,817 | A/T | missense variant | — |
| rs1259153585 | 2:203,846,820 | C/T | — | uncertain significance |
| rs75249727 | 2:203,846,865 | C/T | — | benign |
| rs369165369 | 2:203,846,898 | T/C | — | uncertain significance |
| rs2105946935 | 2:203,846,909 | G/T | — | uncertain significance |
| rs754701730 | 2:203,846,927 | C/A | — | uncertain significance |
| rs1369939183 | 2:203,846,972 | A/T | — | uncertain significance |
| rs201017244 | 2:203,847,008 | C/T | — | uncertain significance |
| rs201737264 | 2:203,847,024 | A/C | — | uncertain significance |
| rs751698433 | 2:203,847,075 | C/T | — | uncertain significance |
| rs201292369 | 2:203,847,101 | C/T | — | uncertain significance |
| rs554151513 | 2:203,848,240 | C/T | — | uncertain significance |
| rs770541757 | 2:203,848,313 | A/C | — | uncertain significance |
| rs2060351118 | 2:203,848,330 | A/G | — | uncertain significance |
| rs114118372 | 2:203,848,342 | A/G | — | benign |
| rs62183749 | 2:203,848,724 | G/A | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.