IGDCC3
immunoglobulin superfamily DCC subclass member 3
Summary
Predicted to be involved in cell-cell adhesion. Predicted to act upstream of or within neuromuscular process controlling balance. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201621281 | 15:65,621,342 | G/A | — | uncertain significance |
| rs1214935054 | 15:65,621,351 | C/G | — | uncertain significance |
| rs752264561 | 15:65,621,374 | G/A | — | uncertain significance |
| rs1480735929 | 15:65,621,401 | G/A | — | uncertain significance |
| rs201058521 | 15:65,621,427 | C/A | — | uncertain significance |
| rs1595747630 | 15:65,621,453 | T/A | — | uncertain significance |
| rs768491748 | 15:65,621,772 | A/G | — | uncertain significance |
| rs147682774 | 15:65,621,801 | C/T | — | likely benign |
| rs767194741 | 15:65,621,850 | T/G | — | uncertain significance |
| rs758579816 | 15:65,621,867 | G/A | — | uncertain significance |
| rs766501573 | 15:65,621,882 | C/T | — | uncertain significance |
| rs140847375 | 15:65,622,077 | C/T | — | uncertain significance |
| rs776056063 | 15:65,622,178 | C/T | — | uncertain significance |
| rs769953396 | 15:65,622,667 | G/A | — | uncertain significance |
| rs2090967535 | 15:65,622,902 | T/C | — | uncertain significance |
| rs746790782 | 15:65,622,915 | C/T | — | uncertain significance |
| rs16948657 | 15:65,622,916 | G/A | — | benign |
| rs370445081 | 15:65,622,939 | C/T | — | uncertain significance |
| rs573108336 | 15:65,622,990 | C/T | — | uncertain significance |
| rs143782720 | 15:65,623,053 | G/C | — | uncertain significance |
| rs1382372954 | 15:65,623,780 | C/T | — | uncertain significance |
| rs145775314 | 15:65,623,805 | C/T | — | likely benign |
| rs200817130 | 15:65,623,854 | C/T | — | likely benign |
| rs766994812 | 15:65,623,855 | G/A | — | uncertain significance |
| rs146744299 | 15:65,623,897 | C/T | — | uncertain significance |
| rs145612224 | 15:65,623,939 | C/T | — | uncertain significance |
| rs201766054 | 15:65,623,975 | C/T | — | uncertain significance |
| rs756418199 | 15:65,624,301 | C/T | — | uncertain significance |
| rs749325757 | 15:65,624,312 | G/A | — | uncertain significance |
| rs771817257 | 15:65,624,324 | T/C | — | uncertain significance |
| rs567453871 | 15:65,624,342 | G/A | — | uncertain significance |
| rs373957008 | 15:65,624,352 | G/A | — | uncertain significance |
| rs201324823 | 15:65,624,354 | G/A | — | uncertain significance |
| rs79857588 | 15:65,625,683 | C/T | — | benign |
| rs376775861 | 15:65,627,092 | C/T | — | uncertain significance |
| rs918855313 | 15:65,627,101 | C/T | — | uncertain significance |
| rs112189384 | 15:65,627,210 | G/A | — | benign |
| rs2542422278 | 15:65,627,635 | C/T | — | uncertain significance |
| rs2542422394 | 15:65,627,686 | C/T | — | uncertain significance |
| rs1405894608 | 15:65,627,746 | G/A | — | uncertain significance |
| rs142065230 | 15:65,628,163 | T/A | — | uncertain significance |
| rs547234144 | 15:65,657,513 | G/A | — | — |
| rs545378604 | 15:65,666,785 | A/T | — | — |
| rs376189801 | 15:65,667,458 | C/T | — | uncertain significance |
| rs2542456626 | 15:65,667,551 | A/G | — | uncertain significance |
| rs780584742 | 15:65,667,564 | C/T | — | uncertain significance |
| rs113171100 | 15:65,667,592 | C/A | — | uncertain significance |
| rs74349672 | 15:65,667,690 | C/T | — | benign |
| rs1360193288 | 15:65,667,729 | A/G | — | uncertain significance |
| rs72625758 | 15:65,667,933 | T/C | intron variant | — |
| rs2091368259 | 15:65,670,053 | A/C | — | uncertain significance |
| rs576557987 | 15:65,670,054 | G/T | — | uncertain significance |
| rs1398168887 | 15:65,670,083 | G/C | — | uncertain significance |
| rs919586975 | 15:65,670,086 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.