COBLL1
cordon-bleu WH2 repeat protein like 1
Summary
Enables cadherin binding activity. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants88 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs75265117 | 2:165,518,799 | C/G | intron variant | — |
| rs62173904 | 2:165,524,499 | G/T | — | — |
| rs36105243 | 2:165,524,751 | C/G | intron variant | — |
| rs13432797 | 2:165,526,587 | G/C | intron variant | — |
| rs13389219 | 2:165,528,876 | C/T | regulatory region variant | — |
| rs6717858 | 2:165,539,661 | T/A | — | — |
| rs12328675 | 2:165,540,800 | T/C | downstream gene variant | — |
| rs11558901 | 2:165,541,308 | A/T | downstream gene variant | — |
| rs6738627 | 2:165,544,450 | G/A | upstream gene variant | — |
| rs115743734 | 2:165,547,355 | G/A | upstream gene variant | — |
| rs2467920560 | 2:165,548,826 | T/C | — | uncertain significance |
| rs936989379 | 2:165,550,825 | G/T | — | uncertain significance |
| rs112597395 | 2:165,550,888 | T/G | — | uncertain significance |
| rs368932917 | 2:165,550,895 | G/A | — | uncertain significance |
| rs377299562 | 2:165,550,904 | T/G | — | uncertain significance |
| rs369559674 | 2:165,550,942 | G/A | — | uncertain significance |
| rs1026571533 | 2:165,551,053 | G/T | — | uncertain significance |
| rs756784317 | 2:165,551,084 | C/T | — | likely benign |
| rs771398593 | 2:165,551,183 | C/T | — | uncertain significance |
| rs2467928834 | 2:165,551,192 | C/T | — | uncertain significance |
| rs7607980 | 2:165,551,201 | T/C | missense variant | — |
| rs376126585 | 2:165,551,231 | C/T | — | uncertain significance |
| rs147994447 | 2:165,551,275 | G/A | — | uncertain significance |
| rs199845314 | 2:165,551,281 | C/G | — | uncertain significance |
| rs141706142 | 2:165,551,327 | T/C | — | uncertain significance |
| rs2105430255 | 2:165,551,456 | C/T | — | uncertain significance |
| rs148954553 | 2:165,551,476 | G/A | — | uncertain significance |
| rs560492547 | 2:165,551,502 | A/C | — | likely benign |
| rs773538509 | 2:165,551,586 | A/T | — | uncertain significance |
| rs201545061 | 2:165,551,597 | T/G | — | uncertain significance |
| rs919369972 | 2:165,551,699 | T/C | — | uncertain significance |
| rs1030024838 | 2:165,551,704 | G/A | — | uncertain significance |
| rs371827575 | 2:165,551,705 | T/C | — | uncertain significance |
| rs189600717 | 2:165,551,864 | G/T | — | uncertain significance |
| rs1298904878 | 2:165,551,882 | T/C | — | uncertain significance |
| rs201427085 | 2:165,551,893 | G/A | — | uncertain significance |
| rs369864612 | 2:165,552,015 | T/A | — | uncertain significance |
| rs146060190 | 2:165,552,043 | T/C | — | uncertain significance |
| rs748647602 | 2:165,552,140 | C/T | — | uncertain significance |
| rs569020159 | 2:165,552,188 | T/C | — | uncertain significance |
| rs766481813 | 2:165,552,194 | T/G | — | uncertain significance |
| rs534277685 | 2:165,552,259 | C/T | — | uncertain significance |
| rs78970517 | 2:165,554,302 | C/T | regulatory region variant | — |
| rs12692737 | 2:165,554,309 | C/A | regulatory region variant | — |
| rs148013206 | 2:165,555,954 | T/C | — | likely benign |
| rs532465805 | 2:165,555,969 | T/G | — | uncertain significance |
| rs2467946128 | 2:165,555,977 | T/C | — | uncertain significance |
| rs1318837288 | 2:165,555,986 | T/A | — | uncertain significance |
| rs1236151484 | 2:165,556,005 | G/C | — | uncertain significance |
| rs771033458 | 2:165,557,061 | T/A | — | uncertain significance |
| rs377116547 | 2:165,557,120 | C/A | — | uncertain significance |
| rs757127724 | 2:165,557,134 | T/A | — | uncertain significance |
| rs1553469541 | 2:165,557,223 | C/A | — | uncertain significance |
| rs768000842 | 2:165,557,260 | A/C | — | uncertain significance |
| rs760401338 | 2:165,557,263 | C/T | — | uncertain significance |
| rs566596164 | 2:165,558,215 | G/C | — | — |
| rs2467959602 | 2:165,559,641 | G/A | — | uncertain significance |
| rs762591817 | 2:165,559,716 | C/T | — | uncertain significance |
| rs755524405 | 2:165,560,960 | T/C | — | uncertain significance |
| rs149882271 | 2:165,561,470 | C/T | — | likely benign |
| rs778472560 | 2:165,561,471 | G/A | — | uncertain significance |
| rs368417754 | 2:165,561,483 | C/G | — | uncertain significance |
| rs756718050 | 2:165,561,564 | T/C | — | uncertain significance |
| rs3820981 | 2:165,566,877 | A/G | regulatory region variant | — |
| rs141402519 | 2:165,567,120 | G/T | intron variant | — |
| rs10221833 | 2:165,577,164 | G/C | regulatory region variant | — |
| rs779126443 | 2:165,578,604 | C/T | — | uncertain significance |
| rs775742088 | 2:165,578,632 | G/A | — | uncertain significance |
| rs370133485 | 2:165,578,685 | G/A | — | uncertain significance |
| rs770148857 | 2:165,578,724 | G/A | — | uncertain significance |
| rs146718898 | 2:165,578,742 | T/C | — | uncertain significance |
| rs199918655 | 2:165,578,794 | C/T | — | likely benign |
| rs2468032072 | 2:165,584,548 | G/C | — | uncertain significance |
| rs765495430 | 2:165,584,589 | G/A | — | uncertain significance |
| rs201066001 | 2:165,584,691 | A/G | — | uncertain significance |
| rs1452893967 | 2:165,586,477 | T/C | — | uncertain significance |
| rs372953085 | 2:165,586,545 | G/A | — | uncertain significance |
| rs146685683 | 2:165,586,561 | T/C | — | uncertain significance |
| rs370618761 | 2:165,600,203 | T/C | — | uncertain significance |
| rs1686715715 | 2:165,600,257 | T/A | — | uncertain significance |
| rs430419 | 2:165,610,498 | C/T | intron variant | — |
| rs355897 | 2:165,636,332 | T/A | — | — |
| rs355901 | 2:165,639,847 | T/C | intron variant | — |
| rs355906 | 2:165,642,448 | G/T | — | — |
| rs355914 | 2:165,656,787 | G/C | intron variant | — |
| rs200661313 | 2:165,673,886 | A/G | — | — |
| rs113702130 | 2:165,697,678 | T/C | — | uncertain significance |
| rs1683584827 | 2:165,697,679 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.