C1QTNF7
C1q and TNF related 7
Summary
Predicted to enable identical protein binding activity. Predicted to be located in extracellular space. Predicted to be part of collagen trimer. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs114133078 | 4:15,354,385 | T/C | intron variant | — |
| rs191195594 | 4:15,375,360 | C/T | regulatory region variant | — |
| rs139878157 | 4:15,390,223 | G/A | intron variant | — |
| rs16891867 | 4:15,397,364 | A/G | intron variant | — |
| rs13106702 | 4:15,397,450 | A/G | intron variant | — |
| rs1861046 | 4:15,397,906 | G/C | — | — |
| rs554238218 | 4:15,408,174 | T/G | — | — |
| rs547952340 | 4:15,428,576 | T/C | — | — |
| rs77194060 | 4:15,436,150 | G/C | regulatory region variant | — |
| rs140840563 | 4:15,437,367 | G/C | — | uncertain significance |
| rs764617258 | 4:15,437,412 | T/G | — | uncertain significance |
| rs779357256 | 4:15,437,422 | C/T | — | uncertain significance |
| rs760065898 | 4:15,437,503 | C/G | — | uncertain significance |
| rs765869930 | 4:15,437,519 | C/G | — | uncertain significance |
| rs201991320 | 4:15,437,521 | C/T | — | uncertain significance |
| rs201267114 | 4:15,437,531 | A/C | — | uncertain significance |
| rs137951137 | 4:15,437,537 | G/A | — | uncertain significance |
| rs759725235 | 4:15,437,569 | G/A | — | uncertain significance |
| rs114277009 | 4:15,439,864 | A/T | intron variant | — |
| rs2474762381 | 4:15,443,888 | A/T | — | uncertain significance |
| rs1196795024 | 4:15,443,911 | C/G | — | uncertain significance |
| rs748587603 | 4:15,443,954 | G/A | — | uncertain significance |
| rs2474762784 | 4:15,443,971 | A/G | — | uncertain significance |
| rs754147606 | 4:15,444,013 | A/G | — | uncertain significance |
| rs1291046639 | 4:15,444,051 | A/G | — | uncertain significance |
| rs753589539 | 4:15,444,149 | T/C | — | uncertain significance |
| rs199762846 | 4:15,444,220 | G/A | — | uncertain significance |
| rs550036426 | 4:15,444,273 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.