IGDCC4
immunoglobulin superfamily DCC subclass member 4
Summary
Predicted to be involved in cell-cell adhesion. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants90 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2542467761 | 15:65,676,357 | G/T | — | uncertain significance |
| rs143179618 | 15:65,676,385 | G/A | — | likely benign |
| rs751661640 | 15:65,676,523 | C/T | — | uncertain significance |
| rs1384168337 | 15:65,676,534 | A/G | — | uncertain significance |
| rs777638578 | 15:65,676,541 | A/C | — | uncertain significance |
| rs552095729 | 15:65,676,670 | C/T | — | uncertain significance |
| rs757195707 | 15:65,677,297 | T/C | — | uncertain significance |
| rs1401687303 | 15:65,677,329 | G/A | — | uncertain significance |
| rs548109593 | 15:65,677,348 | G/T | — | uncertain significance |
| rs779710828 | 15:65,677,350 | G/A | — | uncertain significance |
| rs2277581 | 15:65,677,459 | C/G | — | benign |
| rs11638938 | 15:65,677,653 | T/C | regulatory region variant | — |
| rs1211965218 | 15:65,678,188 | C/T | — | uncertain significance |
| rs2542474702 | 15:65,678,260 | G/A | — | uncertain significance |
| rs1233052296 | 15:65,678,281 | T/G | — | uncertain significance |
| rs753282771 | 15:65,678,290 | G/A | — | uncertain significance |
| rs778101671 | 15:65,678,320 | G/T | — | uncertain significance |
| rs200433662 | 15:65,678,324 | G/T | — | uncertain significance |
| rs764073649 | 15:65,678,905 | G/A | — | uncertain significance |
| rs146782532 | 15:65,678,959 | C/T | — | uncertain significance |
| rs769406637 | 15:65,678,977 | A/G | — | uncertain significance |
| rs2091481938 | 15:65,680,852 | G/A | — | likely benign |
| rs202023951 | 15:65,680,879 | C/T | — | uncertain significance |
| rs200113249 | 15:65,680,886 | C/T | — | uncertain significance |
| rs772398561 | 15:65,681,184 | G/A | — | uncertain significance |
| rs1191516234 | 15:65,681,218 | C/T | — | uncertain significance |
| rs138139328 | 15:65,681,227 | C/T | — | uncertain significance |
| rs2542482295 | 15:65,681,244 | G/A | — | uncertain significance |
| rs779134142 | 15:65,681,260 | G/C | — | uncertain significance |
| rs144033948 | 15:65,681,640 | G/A | — | uncertain significance |
| rs2542485113 | 15:65,682,578 | A/G | — | uncertain significance |
| rs753949820 | 15:65,682,595 | C/T | — | uncertain significance |
| rs185266355 | 15:65,682,635 | C/T | — | uncertain significance |
| rs139423668 | 15:65,684,226 | G/A | — | uncertain significance |
| rs776932088 | 15:65,684,229 | G/A | — | uncertain significance |
| rs1046463736 | 15:65,684,272 | C/T | — | uncertain significance |
| rs757913847 | 15:65,684,562 | G/A | — | uncertain significance |
| rs1317421398 | 15:65,684,588 | C/T | — | uncertain significance |
| rs373976279 | 15:65,684,655 | C/T | — | uncertain significance |
| rs2542492826 | 15:65,685,715 | C/T | — | uncertain significance |
| rs777874300 | 15:65,685,731 | T/A | — | uncertain significance |
| rs200495254 | 15:65,685,818 | T/A | — | uncertain significance |
| rs150437562 | 15:65,685,845 | C/T | — | uncertain significance |
| rs528209903 | 15:65,686,763 | C/A | — | uncertain significance |
| rs753949741 | 15:65,686,767 | A/G | — | uncertain significance |
| rs1595781043 | 15:65,686,846 | G/C | — | uncertain significance |
| rs2542500215 | 15:65,687,461 | G/T | — | uncertain significance |
| rs775122408 | 15:65,687,471 | G/A | — | uncertain significance |
| rs554878224 | 15:65,687,501 | C/A | — | uncertain significance |
| rs115373732 | 15:65,687,553 | G/A | — | likely benign |
| rs112710889 | 15:65,688,095 | C/T | — | likely benign |
| rs769522572 | 15:65,688,127 | G/T | — | uncertain significance |
| rs146624616 | 15:65,688,169 | C/A | — | uncertain significance |
| rs2062919621 | 15:65,688,209 | G/T | — | uncertain significance |
| rs2542504806 | 15:65,688,247 | C/T | — | uncertain significance |
| rs2542505018 | 15:65,688,261 | A/G | — | likely benign |
| rs1478521711 | 15:65,688,369 | G/A | — | uncertain significance |
| rs950583112 | 15:65,688,414 | G/C | — | uncertain significance |
| rs957450086 | 15:65,688,456 | C/G | — | uncertain significance |
| rs1283965613 | 15:65,689,225 | T/C | — | uncertain significance |
| rs2062977599 | 15:65,693,170 | G/A | — | uncertain significance |
| rs773340207 | 15:65,693,255 | C/G | — | uncertain significance |
| rs377547195 | 15:65,694,704 | T/C | — | uncertain significance |
| rs143723846 | 15:65,694,752 | C/T | — | uncertain significance |
| rs1330506172 | 15:65,694,821 | T/C | — | uncertain significance |
| rs57546763 | 15:65,702,521 | C/A | — | uncertain significance |
| rs765397844 | 15:65,702,538 | C/A | — | uncertain significance |
| rs750478576 | 15:65,702,544 | C/T | — | uncertain significance |
| rs148432274 | 15:65,702,559 | T/C | — | uncertain significance |
| rs1213428098 | 15:65,702,568 | C/T | — | uncertain significance |
| rs367644742 | 15:65,702,595 | A/T | — | uncertain significance |
| rs748008063 | 15:65,702,597 | C/T | — | uncertain significance |
| rs1395798295 | 15:65,702,607 | C/T | — | uncertain significance |
| rs146119608 | 15:65,702,652 | C/T | — | uncertain significance |
| rs759892343 | 15:65,703,402 | G/C | — | uncertain significance |
| rs199723005 | 15:65,703,406 | C/A | — | uncertain significance |
| rs377304189 | 15:65,703,417 | C/A | — | uncertain significance |
| rs146884530 | 15:65,703,447 | G/C | — | uncertain significance |
| rs2547835071 | 15:65,703,463 | C/T | — | uncertain significance |
| rs1291136259 | 15:65,703,474 | T/C | — | uncertain significance |
| rs149985570 | 15:65,703,514 | G/A | — | uncertain significance |
| rs2140233655 | 15:65,703,604 | G/C | — | uncertain significance |
| rs142198652 | 15:65,703,646 | C/T | — | likely benign |
| rs760266345 | 15:65,703,670 | T/A | — | uncertain significance |
| rs2063205820 | 15:65,715,133 | C/A | — | uncertain significance |
| rs576529626 | 15:65,715,153 | G/C | — | likely benign |
| rs957582282 | 15:65,715,175 | C/T | — | uncertain significance |
| rs1010361561 | 15:65,715,178 | C/T | — | uncertain significance |
| rs372599124 | 15:65,715,182 | C/A | — | uncertain significance |
| rs755306114 | 15:65,715,188 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.