CDHR4
cadherin related family member 4
Summary
Predicted to enable calcium ion binding activity. Predicted to be involved in cell adhesion. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs764180294 | 3:49,828,315 | C/T | — | uncertain significance |
| rs145439991 | 3:49,828,863 | G/T | — | — |
| rs1020309463 | 3:49,828,880 | C/T | — | uncertain significance |
| rs755391037 | 3:49,829,148 | A/G | — | uncertain significance |
| rs1236274640 | 3:49,829,153 | C/T | — | uncertain significance |
| rs1251873380 | 3:49,829,191 | G/A | — | uncertain significance |
| rs576389329 | 3:49,829,209 | C/T | — | uncertain significance |
| rs79201191 | 3:49,829,234 | G/C | — | uncertain significance |
| rs1310635142 | 3:49,829,351 | G/A | — | uncertain significance |
| rs775219473 | 3:49,829,383 | C/G | — | uncertain significance |
| rs779968203 | 3:49,830,391 | C/T | — | uncertain significance |
| rs34160951 | 3:49,830,425 | C/T | synonymous variant | — |
| rs2081205995 | 3:49,830,481 | G/C | — | uncertain significance |
| rs758571175 | 3:49,830,600 | C/G | — | uncertain significance |
| rs1230342195 | 3:49,830,626 | T/C | — | uncertain significance |
| rs1029792092 | 3:49,830,674 | C/T | — | likely benign |
| rs973732284 | 3:49,830,728 | G/A | — | uncertain significance |
| rs766303363 | 3:49,831,064 | G/C | — | uncertain significance |
| rs1055164456 | 3:49,831,067 | C/G | — | uncertain significance |
| rs949291183 | 3:49,831,086 | A/G | — | likely benign |
| rs2544878626 | 3:49,831,092 | A/G | — | uncertain significance |
| rs748437703 | 3:49,831,316 | G/A | — | likely benign |
| rs1156542501 | 3:49,831,322 | A/G | — | uncertain significance |
| rs924219022 | 3:49,831,326 | C/T | — | uncertain significance |
| rs753808280 | 3:49,831,352 | G/A | — | uncertain significance |
| rs1053583848 | 3:49,831,353 | C/G | — | uncertain significance |
| rs570035138 | 3:49,831,368 | G/A | — | uncertain significance |
| rs34735338 | 3:49,831,698 | G/A | intron variant | — |
| rs755426003 | 3:49,832,411 | G/C | — | uncertain significance |
| rs767933275 | 3:49,832,429 | C/T | — | likely benign |
| rs2544885628 | 3:49,832,451 | G/C | — | uncertain significance |
| rs1195003292 | 3:49,832,499 | C/T | — | uncertain significance |
| rs757390031 | 3:49,832,653 | G/A | — | uncertain significance |
| rs377496848 | 3:49,832,692 | T/C | — | uncertain significance |
| rs2081252713 | 3:49,832,711 | A/G | — | uncertain significance |
| rs546996057 | 3:49,832,727 | A/C | — | uncertain significance |
| rs1450180004 | 3:49,832,732 | C/G | — | uncertain significance |
| rs888658531 | 3:49,832,780 | C/G | — | uncertain significance |
| rs747880395 | 3:49,832,797 | C/T | — | likely benign |
| rs538987853 | 3:49,832,806 | C/T | — | uncertain significance |
| rs1184140934 | 3:49,833,069 | A/G | — | uncertain significance |
| rs1228258488 | 3:49,833,112 | G/A | — | uncertain significance |
| rs932405794 | 3:49,833,118 | C/T | — | uncertain significance |
| rs554908956 | 3:49,833,154 | C/T | — | uncertain significance |
| rs772919585 | 3:49,833,196 | C/T | — | uncertain significance |
| rs2544891340 | 3:49,833,479 | C/T | — | uncertain significance |
| rs2544894763 | 3:49,834,402 | C/T | — | uncertain significance |
| rs71324996 | 3:49,834,767 | A/C | intron variant | — |
| rs757284426 | 3:49,836,306 | G/A | — | uncertain significance |
| rs2544902621 | 3:49,836,451 | A/G | — | uncertain significance |
| rs199525526 | 3:49,836,471 | C/T | — | uncertain significance |
| rs762170080 | 3:49,836,685 | C/T | — | uncertain significance |
| rs763666592 | 3:49,836,816 | G/A | — | uncertain significance |
| rs1284523959 | 3:49,837,211 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.