MAGI3
membrane associated guanylate kinase, WW and PDZ domain containing 3
Summary
Predicted to enable frizzled binding activity. Predicted to be involved in signal transduction. Predicted to act upstream of or within positive regulation of JUN kinase activity. Located in cell junction. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants80 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2526263977 | 1:113,933,735 | G/T | — | uncertain significance |
| rs551196385 | 1:113,933,795 | G/A | — | uncertain significance |
| rs1033304573 | 1:113,933,837 | C/G | — | uncertain significance |
| rs1039496686 | 1:113,933,914 | A/G | — | uncertain significance |
| rs1112085 | 1:113,941,165 | G/C | — | — |
| rs12024428 | 1:113,957,385 | A/G | intron variant | — |
| rs12030900 | 1:113,974,263 | A/G | intron variant | — |
| rs146750254 | 1:113,980,577 | T/C | intron variant | — |
| rs11102637 | 1:113,991,792 | G/A | upstream gene variant | — |
| rs377112211 | 1:114,078,776 | T/A | — | — |
| rs376671198 | 1:114,078,779 | T/A | — | — |
| rs772074544 | 1:114,092,161 | G/A | — | uncertain significance |
| rs376619517 | 1:114,092,196 | A/G | — | uncertain significance |
| rs1343125 | 1:114,111,036 | A/G | intron variant | — |
| rs112936545 | 1:114,118,802 | C/A | — | — |
| rs35955172 | 1:114,128,124 | G/A | — | benign |
| rs2526987391 | 1:114,133,180 | A/G | — | uncertain significance |
| rs771362682 | 1:114,133,250 | A/G | — | uncertain significance |
| rs534911859 | 1:114,133,264 | A/T | — | uncertain significance |
| rs1383066015 | 1:114,137,174 | A/C | — | uncertain significance |
| rs771970427 | 1:114,137,176 | G/A | — | uncertain significance |
| rs188006969 | 1:114,152,453 | T/A | intron variant | — |
| rs1342731814 | 1:114,162,402 | C/G | — | uncertain significance |
| rs200650478 | 1:114,165,472 | G/A | — | uncertain significance |
| rs41283512 | 1:114,165,485 | G/A | — | uncertain significance |
| rs145442738 | 1:114,165,506 | C/T | — | uncertain significance |
| rs778592316 | 1:114,165,508 | A/G | — | uncertain significance |
| rs1230666 | 1:114,173,410 | A/G | intron variant | — |
| rs772403961 | 1:114,184,572 | G/C | — | uncertain significance |
| rs1245755372 | 1:114,184,597 | G/T | — | uncertain significance |
| rs1161778440 | 1:114,184,760 | G/T | — | uncertain significance |
| rs767631910 | 1:114,184,803 | C/T | — | uncertain significance |
| rs768556553 | 1:114,185,084 | G/A | — | uncertain significance |
| rs761476097 | 1:114,185,094 | A/G | — | uncertain significance |
| rs776447798 | 1:114,186,368 | C/T | — | uncertain significance |
| rs12144215 | 1:114,187,155 | G/T | intron variant | — |
| rs369633891 | 1:114,189,153 | G/C | — | uncertain significance |
| rs371336059 | 1:114,189,184 | C/A | — | uncertain significance |
| rs1170440264 | 1:114,189,201 | G/C | — | uncertain significance |
| rs2524677973 | 1:114,189,250 | T/C | — | uncertain significance |
| rs542583012 | 1:114,189,263 | A/T | — | uncertain significance |
| rs775683003 | 1:114,191,892 | G/A | — | uncertain significance |
| rs762112637 | 1:114,193,651 | A/G | — | uncertain significance |
| rs759189272 | 1:114,193,685 | G/C | — | uncertain significance |
| rs372270961 | 1:114,193,690 | C/T | — | uncertain significance |
| rs142998380 | 1:114,193,691 | G/A | — | likely benign |
| rs780357245 | 1:114,193,696 | G/T | — | uncertain significance |
| rs2524693333 | 1:114,193,774 | G/T | — | uncertain significance |
| rs367730325 | 1:114,193,823 | A/G | — | uncertain significance |
| rs867000529 | 1:114,196,469 | G/A | — | uncertain significance |
| rs144491494 | 1:114,196,553 | G/A | — | uncertain significance |
| rs753459456 | 1:114,196,576 | A/T | — | uncertain significance |
| rs980239363 | 1:114,201,849 | C/G | — | uncertain significance |
| rs150230904 | 1:114,214,359 | A/T | — | uncertain significance |
| rs138270035 | 1:114,214,371 | C/T | — | uncertain significance |
| rs754672993 | 1:114,215,306 | G/C | — | uncertain significance |
| rs905894975 | 1:114,215,983 | C/T | — | uncertain significance |
| rs1295683728 | 1:114,223,908 | A/G | — | uncertain significance |
| rs1381086911 | 1:114,225,621 | A/T | — | uncertain significance |
| rs538666966 | 1:114,225,635 | G/A | — | uncertain significance |
| rs2524783625 | 1:114,225,641 | T/A | — | uncertain significance |
| rs61751950 | 1:114,225,692 | C/G | — | uncertain significance |
| rs2524783875 | 1:114,225,704 | A/T | — | uncertain significance |
| rs777676148 | 1:114,225,718 | A/T | — | uncertain significance |
| rs571333192 | 1:114,225,796 | C/G | — | uncertain significance |
| rs773553087 | 1:114,225,810 | A/C | — | uncertain significance |
| rs770451764 | 1:114,225,852 | C/T | — | uncertain significance |
| rs1398929146 | 1:114,225,887 | G/C | — | uncertain significance |
| rs1648336936 | 1:114,225,987 | G/A | — | uncertain significance |
| rs567321137 | 1:114,226,049 | G/C | — | uncertain significance |
| rs1241078853 | 1:114,226,122 | G/T | — | uncertain significance |
| rs1223600506 | 1:114,226,125 | A/G | — | uncertain significance |
| rs61742849 | 1:114,226,143 | G/C | missense variant | — |
| rs372079100 | 1:114,226,149 | C/T | — | uncertain significance |
| rs61742852 | 1:114,226,153 | C/T | — | benign |
| rs757765777 | 1:114,226,193 | G/A | — | uncertain significance |
| rs750779760 | 1:114,226,196 | G/A | — | uncertain significance |
| rs375686992 | 1:114,226,529 | G/C | — | uncertain significance |
| rs766953489 | 1:114,226,604 | G/C | — | uncertain significance |
| rs758601731 | 1:114,226,629 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.