C1QTNF6
C1q and TNF related 6
Summary
Enables identical protein binding activity. Predicted to be located in extracellular region and membrane. Predicted to be part of collagen trimer. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs140234868 | 22:37,578,233 | C/T | — | uncertain significance |
| rs201178136 | 22:37,578,308 | G/A | — | uncertain significance |
| rs148769820 | 22:37,578,380 | T/C | — | uncertain significance |
| rs369130130 | 22:37,578,392 | C/T | — | uncertain significance |
| rs201190967 | 22:37,578,419 | C/T | — | uncertain significance |
| rs2517871380 | 22:37,578,469 | C/T | — | uncertain significance |
| rs199739157 | 22:37,578,502 | C/T | — | uncertain significance |
| rs140887252 | 22:37,578,524 | C/T | — | uncertain significance |
| rs779497510 | 22:37,578,568 | T/C | — | uncertain significance |
| rs1398111940 | 22:37,578,577 | A/G | — | uncertain significance |
| rs370547311 | 22:37,578,593 | C/T | — | uncertain significance |
| rs986273635 | 22:37,578,656 | C/T | — | uncertain significance |
| rs2517872646 | 22:37,578,727 | C/T | — | likely benign |
| rs569663804 | 22:37,578,736 | T/A | — | uncertain significance |
| rs77643619 | 22:37,581,271 | G/A | — | benign |
| rs140874536 | 22:37,581,279 | T/C | — | uncertain significance |
| rs747547190 | 22:37,581,355 | G/T | — | uncertain significance |
| rs1434189212 | 22:37,581,384 | C/T | — | uncertain significance |
| rs200314628 | 22:37,581,420 | T/C | — | uncertain significance |
| rs229526 | 22:37,581,422 | G/T | missense variant | — |
| rs112360472 | 22:37,581,433 | C/A | — | uncertain significance |
| rs138910187 | 22:37,581,457 | T/C | — | benign |
| rs229527 | 22:37,581,485 | C/A | missense variant | — |
| rs747027209 | 22:37,584,235 | G/A | — | uncertain significance |
| rs2160908 | 22:37,586,792 | C/T | upstream gene variant | — |
| rs229533 | 22:37,587,111 | A/C | upstream gene variant | — |
| rs6000602 | 22:37,590,549 | C/A | intron variant | — |
| rs229541 | 22:37,591,318 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.