PDZRN4
PDZ domain containing ring finger 4
Summary
Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants86 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2498205258 | 12:41,582,307 | A/G | — | uncertain significance |
| rs764685437 | 12:41,582,322 | G/A | — | uncertain significance |
| rs752180193 | 12:41,582,336 | G/C | — | uncertain significance |
| rs936685241 | 12:41,582,387 | C/T | — | uncertain significance |
| rs1950710157 | 12:41,582,428 | G/T | — | uncertain significance |
| rs1473458484 | 12:41,582,438 | C/G | — | uncertain significance |
| rs537582782 | 12:41,582,529 | C/T | — | uncertain significance |
| rs2498206025 | 12:41,582,535 | G/A | — | uncertain significance |
| rs773834197 | 12:41,582,564 | C/G | — | uncertain significance |
| rs1245517294 | 12:41,582,582 | G/A | — | uncertain significance |
| rs549946808 | 12:41,582,588 | C/G | — | uncertain significance |
| rs754649260 | 12:41,582,598 | G/A | — | uncertain significance |
| rs776949471 | 12:41,582,604 | G/C | — | uncertain significance |
| rs765431849 | 12:41,582,607 | G/C | — | uncertain significance |
| rs572012656 | 12:41,582,651 | G/A | — | uncertain significance |
| rs539005475 | 12:41,582,661 | C/G | — | uncertain significance |
| rs2498207097 | 12:41,582,691 | C/A | — | uncertain significance |
| rs2498207175 | 12:41,582,717 | T/G | — | uncertain significance |
| rs543178354 | 12:41,582,816 | C/T | — | uncertain significance |
| rs1203666366 | 12:41,582,873 | T/A | — | uncertain significance |
| rs117626015 | 12:41,624,795 | T/C | intron variant | — |
| rs529929509 | 12:41,651,348 | C/T | — | — |
| rs10785188 | 12:41,651,953 | A/C | — | — |
| rs1880887 | 12:41,721,430 | C/G | — | — |
| rs1317540 | 12:41,731,749 | T/A | intron variant | — |
| rs73126876 | 12:41,777,246 | A/C | intron variant | — |
| rs7133365 | 12:41,801,963 | T/A | downstream gene variant | — |
| rs2733289 | 12:41,838,235 | T/C | intron variant | — |
| rs1841025 | 12:41,846,272 | T/G | — | — |
| rs2468315 | 12:41,861,289 | A/C | intron variant | — |
| rs2730827 | 12:41,863,393 | C/T | intron variant | — |
| rs2730806 | 12:41,866,904 | A/G | — | — |
| rs1026464 | 12:41,868,585 | C/A | upstream gene variant | — |
| rs187043470 | 12:41,870,804 | A/C | upstream gene variant | — |
| rs2733287 | 12:41,880,909 | A/G | — | — |
| rs202059222 | 12:41,900,262 | A/G | — | uncertain significance |
| rs542201511 | 12:41,900,321 | A/G | — | uncertain significance |
| rs1333301298 | 12:41,900,369 | C/A | — | uncertain significance |
| rs200204527 | 12:41,900,475 | C/T | — | uncertain significance |
| rs529884020 | 12:41,903,633 | T/A | — | uncertain significance |
| rs370272874 | 12:41,903,657 | A/G | — | uncertain significance |
| rs201184717 | 12:41,903,672 | G/T | — | uncertain significance |
| rs1189839681 | 12:41,903,691 | C/G | — | uncertain significance |
| rs285589 | 12:41,944,407 | T/C | intron variant | — |
| rs140551427 | 12:41,946,516 | G/A | — | uncertain significance |
| rs285582 | 12:41,948,845 | C/G | — | — |
| rs202115349 | 12:41,949,540 | G/A | — | uncertain significance |
| rs148864807 | 12:41,949,552 | G/A | — | uncertain significance |
| rs138003679 | 12:41,961,662 | T/A | — | uncertain significance |
| rs1190632963 | 12:41,961,696 | G/A | — | uncertain significance |
| rs1939404709 | 12:41,961,700 | A/G | — | uncertain significance |
| rs1458175 | 12:41,965,861 | A/T | — | — |
| rs773345137 | 12:41,966,181 | G/A | — | uncertain significance |
| rs932211694 | 12:41,966,194 | C/T | — | uncertain significance |
| rs2498682493 | 12:41,966,260 | A/G | — | uncertain significance |
| rs369918672 | 12:41,966,269 | G/A | — | uncertain significance |
| rs146342073 | 12:41,966,307 | G/A | — | uncertain significance |
| rs1939501465 | 12:41,966,385 | T/A | — | uncertain significance |
| rs151221740 | 12:41,966,438 | C/G | — | uncertain significance |
| rs547346460 | 12:41,966,445 | G/A | — | uncertain significance |
| rs759263589 | 12:41,966,452 | G/C | — | uncertain significance |
| rs777071194 | 12:41,966,508 | T/G | — | uncertain significance |
| rs746524210 | 12:41,966,598 | C/A | — | uncertain significance |
| rs2120864183 | 12:41,966,698 | G/A | — | uncertain significance |
| rs369468806 | 12:41,966,700 | T/A | — | uncertain significance |
| rs2498683822 | 12:41,966,729 | G/A | — | uncertain significance |
| rs757000783 | 12:41,966,764 | C/T | — | uncertain significance |
| rs2498684286 | 12:41,966,950 | C/T | — | uncertain significance |
| rs747380631 | 12:41,967,009 | G/A | — | likely benign |
| rs369306795 | 12:41,967,015 | G/A | — | uncertain significance |
| rs1419780143 | 12:41,967,036 | C/A | — | uncertain significance |
| rs372736876 | 12:41,967,039 | G/A | — | uncertain significance |
| rs149769921 | 12:41,967,043 | A/G | — | uncertain significance |
| rs1367713542 | 12:41,967,069 | C/T | — | uncertain significance |
| rs1301581406 | 12:41,967,075 | C/G | — | uncertain significance |
| rs2498684791 | 12:41,967,184 | G/A | — | uncertain significance |
| rs555539130 | 12:41,967,260 | T/G | — | uncertain significance |
| rs770862484 | 12:41,967,267 | G/A | — | uncertain significance |
| rs1291352004 | 12:41,967,415 | A/C | — | uncertain significance |
| rs2498685661 | 12:41,967,517 | G/C | — | uncertain significance |
| rs370694115 | 12:41,967,529 | A/G | — | uncertain significance |
| rs1939527769 | 12:41,967,559 | A/G | — | uncertain significance |
| rs761096719 | 12:41,967,564 | A/G | — | uncertain significance |
| rs1939528606 | 12:41,967,588 | A/T | — | uncertain significance |
| rs533386950 | 12:41,967,619 | T/G | — | uncertain significance |
| rs747681297 | 12:41,967,661 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.