DCBLD2
discoidin, CUB and LCCL domain containing 2
Summary
Predicted to enable signaling receptor activity. Involved in negative regulation of cell growth and wound healing. Located in cell surface and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs199992795 | 3:98,518,346 | T/C | — | uncertain significance |
| rs200981832 | 3:98,518,359 | G/T | — | uncertain significance |
| rs190117443 | 3:98,518,397 | T/C | — | uncertain significance |
| rs1220312098 | 3:98,518,410 | C/T | — | uncertain significance |
| rs367919009 | 3:98,518,526 | G/A | — | uncertain significance |
| rs111245657 | 3:98,518,530 | T/C | — | likely benign |
| rs767371934 | 3:98,518,545 | C/T | — | uncertain significance |
| rs369665355 | 3:98,518,568 | C/T | — | uncertain significance |
| rs1399302463 | 3:98,518,658 | A/G | — | uncertain significance |
| rs749511785 | 3:98,519,480 | C/T | — | uncertain significance |
| rs199755908 | 3:98,519,494 | C/T | — | uncertain significance |
| rs370426957 | 3:98,519,495 | G/A | — | uncertain significance |
| rs367797096 | 3:98,520,483 | T/G | — | uncertain significance |
| rs540295212 | 3:98,522,050 | C/T | — | — |
| rs201629117 | 3:98,526,982 | A/G | — | uncertain significance |
| rs143662022 | 3:98,530,317 | G/T | — | uncertain significance |
| rs200621366 | 3:98,530,329 | G/A | — | uncertain significance |
| rs907970289 | 3:98,530,350 | T/C | — | uncertain significance |
| rs186169797 | 3:98,530,395 | C/T | — | uncertain significance |
| rs6788689 | 3:98,532,282 | G/A | regulatory region variant | — |
| rs116350450 | 3:98,536,652 | T/C | — | benign |
| rs149988957 | 3:98,536,663 | C/T | — | likely benign |
| rs536126933 | 3:98,536,714 | T/C | — | uncertain significance |
| rs538909861 | 3:98,538,099 | G/A | — | uncertain significance |
| rs200822370 | 3:98,538,112 | C/T | — | uncertain significance |
| rs368134855 | 3:98,538,120 | G/A | — | uncertain significance |
| rs569211029 | 3:98,538,216 | G/A | — | uncertain significance |
| rs200789862 | 3:98,538,222 | G/A | — | uncertain significance |
| rs773751240 | 3:98,538,223 | C/T | — | uncertain significance |
| rs369313436 | 3:98,541,073 | C/T | — | uncertain significance |
| rs773126257 | 3:98,541,085 | C/T | — | uncertain significance |
| rs138571278 | 3:98,542,174 | C/T | downstream gene variant | — |
| rs34234373 | 3:98,552,764 | G/C | — | — |
| rs13083238 | 3:98,564,255 | A/G | intron variant | — |
| rs180752673 | 3:98,568,332 | C/T | — | uncertain significance |
| rs1292295506 | 3:98,568,391 | C/T | — | uncertain significance |
| rs771411018 | 3:98,568,409 | T/C | — | uncertain significance |
| rs10589669 | 3:98,570,148 | G/A | intron variant | — |
| rs140620086 | 3:98,576,311 | C/T | regulatory region variant | — |
| rs541615798 | 3:98,577,187 | G/A | — | — |
| rs143321878 | 3:98,578,670 | C/T | intron variant | — |
| rs142552195 | 3:98,580,955 | A/T | intron variant | — |
| rs9846225 | 3:98,581,826 | C/A | intron variant | — |
| rs2454684 | 3:98,586,309 | T/G | — | — |
| rs181706499 | 3:98,588,964 | G/A | intron variant | — |
| rs184374242 | 3:98,594,153 | C/T | intron variant | — |
| rs189187462 | 3:98,594,781 | C/T | regulatory region variant | — |
| rs9838238 | 3:98,600,385 | T/C | missense variant | — |
| rs750395871 | 3:98,600,482 | C/T | — | uncertain significance |
| rs374307805 | 3:98,600,507 | G/A | — | uncertain significance |
| rs777152672 | 3:98,600,546 | G/T | — | uncertain significance |
| rs34860591 | 3:98,607,464 | T/C | regulatory region variant | — |
| rs1010772028 | 3:98,619,996 | G/A | — | likely benign |
| rs186164278 | 3:98,620,032 | T/C | — | uncertain significance |
| rs368040324 | 3:98,620,037 | A/G | — | likely benign |
| rs2472083893 | 3:98,620,091 | C/T | — | uncertain significance |
| rs1368021708 | 3:98,620,124 | G/A | — | uncertain significance |
| rs1409619844 | 3:98,620,136 | C/A | — | uncertain significance |
| rs532118815 | 3:98,620,158 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.