CNTN3
contactin 3
Summary
Predicted to be involved in cell adhesion. Predicted to be located in extracellular region and plasma membrane. Predicted to be active in neuron projection. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants84 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs946118509 | 3:74,313,562 | A/G | — | likely benign |
| rs147055375 | 3:74,313,584 | C/T | — | benign |
| rs1041987320 | 3:74,313,640 | C/G | — | uncertain significance |
| rs751329291 | 3:74,315,640 | C/T | — | uncertain significance |
| rs1292177190 | 3:74,315,686 | T/C | — | uncertain significance |
| rs765564868 | 3:74,315,722 | T/C | — | uncertain significance |
| rs144881079 | 3:74,315,765 | T/G | — | uncertain significance |
| rs78035726 | 3:74,315,777 | T/C | — | benign |
| rs140717445 | 3:74,316,427 | G/T | — | likely benign |
| rs1464368275 | 3:74,316,451 | G/A | — | uncertain significance |
| rs115651661 | 3:74,321,406 | T/C | intron variant | — |
| rs141921900 | 3:74,334,458 | A/G | — | benign |
| rs556456657 | 3:74,334,476 | T/C | — | uncertain significance |
| rs542742446 | 3:74,334,616 | C/T | — | likely benign |
| rs761438541 | 3:74,334,621 | C/T | — | uncertain significance |
| rs199931035 | 3:74,334,638 | C/T | — | uncertain significance |
| rs764510749 | 3:74,344,295 | T/C | — | uncertain significance |
| rs2471591556 | 3:74,344,313 | T/C | — | uncertain significance |
| rs10490832 | 3:74,344,356 | G/T | — | benign |
| rs2471591757 | 3:74,344,378 | A/T | — | uncertain significance |
| rs1702314931 | 3:74,344,379 | C/G | — | uncertain significance |
| rs1291196687 | 3:74,347,339 | C/G | — | uncertain significance |
| rs543683676 | 3:74,347,347 | A/G | — | likely benign |
| rs626578 | 3:74,349,062 | T/C | — | benign |
| rs1406027887 | 3:74,350,558 | C/T | — | uncertain significance |
| rs915911575 | 3:74,350,570 | T/G | — | uncertain significance |
| rs1227036979 | 3:74,350,573 | C/T | — | uncertain significance |
| rs2471602965 | 3:74,350,596 | C/T | — | uncertain significance |
| rs147790729 | 3:74,350,659 | A/G | — | uncertain significance |
| rs111626135 | 3:74,350,673 | C/T | — | likely benign |
| rs139861462 | 3:74,350,674 | G/A | — | benign |
| rs201998015 | 3:74,350,684 | C/T | — | uncertain significance |
| rs150713791 | 3:74,350,791 | G/A | — | likely benign |
| rs148089886 | 3:74,350,807 | C/T | — | likely benign |
| rs144093273 | 3:74,350,837 | G/A | — | uncertain significance |
| rs74507713 | 3:74,350,869 | T/C | — | benign |
| rs140530465 | 3:74,350,933 | C/T | — | likely benign |
| rs75253024 | 3:74,351,863 | A/T | — | benign |
| rs1400325379 | 3:74,351,882 | C/T | — | uncertain significance |
| rs369703868 | 3:74,351,962 | T/C | — | uncertain significance |
| rs1703348325 | 3:74,383,966 | C/T | — | uncertain significance |
| rs199555851 | 3:74,383,974 | G/A | — | uncertain significance |
| rs920511021 | 3:74,383,982 | T/A | — | uncertain significance |
| rs778468338 | 3:74,384,006 | G/A | — | likely benign |
| rs200087609 | 3:74,384,034 | G/T | — | uncertain significance |
| rs150593292 | 3:74,385,708 | T/G | — | uncertain significance |
| rs200992823 | 3:74,385,712 | C/T | — | likely benign |
| rs1282558849 | 3:74,385,743 | G/A | — | likely benign |
| rs780105765 | 3:74,385,747 | G/C | — | uncertain significance |
| rs1703402417 | 3:74,385,770 | A/T | — | uncertain significance |
| rs769483720 | 3:74,385,800 | C/G | — | likely benign |
| rs2471658286 | 3:74,385,805 | A/T | — | uncertain significance |
| rs200380587 | 3:74,411,057 | C/T | — | uncertain significance |
| rs1420023141 | 3:74,411,186 | C/G | — | uncertain significance |
| rs200432292 | 3:74,413,609 | C/T | — | likely benign |
| rs1559565323 | 3:74,414,725 | C/A | — | uncertain significance |
| rs756569621 | 3:74,414,809 | C/T | — | uncertain significance |
| rs182676092 | 3:74,414,860 | T/C | — | benign |
| rs1704274681 | 3:74,418,348 | G/A | — | uncertain significance |
| rs1418842277 | 3:74,418,355 | G/T | — | uncertain significance |
| rs370041595 | 3:74,418,412 | C/T | — | likely benign |
| rs1025779584 | 3:74,418,431 | G/A | — | likely benign |
| rs2471707273 | 3:74,418,473 | G/T | — | uncertain significance |
| rs62620465 | 3:74,419,065 | T/C | — | benign |
| rs776282929 | 3:74,419,072 | C/T | — | likely benign |
| rs139461362 | 3:74,419,073 | G/A | — | likely benign |
| rs903493578 | 3:74,419,086 | C/T | — | uncertain significance |
| rs2471708493 | 3:74,419,121 | G/T | — | uncertain significance |
| rs760786514 | 3:74,420,355 | C/T | — | uncertain significance |
| rs140108637 | 3:74,420,444 | C/T | — | likely benign |
| rs367688857 | 3:74,420,493 | C/T | — | uncertain significance |
| rs1704333610 | 3:74,420,494 | G/A | — | uncertain significance |
| rs575796079 | 3:74,420,498 | A/C | — | uncertain significance |
| rs1704334074 | 3:74,420,503 | C/T | — | uncertain significance |
| rs1701670872 | 3:74,474,004 | T/C | — | uncertain significance |
| rs758501831 | 3:74,474,089 | G/C | — | uncertain significance |
| rs75740502 | 3:74,474,096 | T/G | — | benign |
| rs554774859 | 3:74,495,440 | T/C | — | — |
| rs79269214 | 3:74,534,902 | A/G | — | — |
| rs374611056 | 3:74,535,738 | C/T | — | uncertain significance |
| rs151030773 | 3:74,535,742 | G/C | — | likely benign |
| rs9879863 | 3:74,548,946 | T/A | — | benign |
| rs13073838 | 3:74,627,703 | T/C | intergenic variant | — |
| rs1374879 | 3:74,635,097 | T/C | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.