CPED1
cadherin like and PC-esterase domain containing 1
Summary
Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants102 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs777151635 | 7:120,629,679 | G/A | — | uncertain significance |
| rs374427830 | 7:120,629,698 | C/T | — | likely benign |
| rs375547307 | 7:120,629,806 | C/G | — | uncertain significance |
| rs935795982 | 7:120,629,886 | T/A | — | uncertain significance |
| rs117047013 | 7:120,629,916 | A/G | — | likely benign |
| rs761912789 | 7:120,655,723 | A/G | — | uncertain significance |
| rs201927951 | 7:120,655,733 | G/A | — | likely benign |
| rs201993865 | 7:120,655,759 | G/A | — | uncertain significance |
| rs1209829099 | 7:120,655,767 | A/T | — | uncertain significance |
| rs1449277888 | 7:120,655,807 | A/C | — | uncertain significance |
| rs999564612 | 7:120,655,827 | A/G | — | uncertain significance |
| rs752999333 | 7:120,655,843 | C/T | — | uncertain significance |
| rs137952014 | 7:120,655,885 | C/T | — | likely benign |
| rs34283669 | 7:120,655,889 | G/A | — | benign |
| rs2485203173 | 7:120,686,946 | C/G | — | uncertain significance |
| rs1793214256 | 7:120,686,971 | G/T | — | uncertain significance |
| rs781375442 | 7:120,686,992 | A/T | — | uncertain significance |
| rs570205413 | 7:120,704,299 | G/T | — | likely benign |
| rs1024743 | 7:120,725,427 | A/C | upstream gene variant | — |
| rs2110281 | 7:120,725,809 | G/A | upstream gene variant | — |
| rs144800578 | 7:120,737,777 | C/G | — | uncertain significance |
| rs2485343369 | 7:120,737,795 | G/A | — | uncertain significance |
| rs1437394271 | 7:120,737,861 | C/G | — | uncertain significance |
| rs200638100 | 7:120,739,988 | C/T | — | uncertain significance |
| rs201996698 | 7:120,740,084 | G/A | — | uncertain significance |
| rs772467238 | 7:120,740,099 | C/T | — | uncertain significance |
| rs2485350403 | 7:120,740,107 | A/C | — | uncertain significance |
| rs113695658 | 7:120,740,109 | A/G | — | benign |
| rs200075911 | 7:120,740,129 | A/T | — | uncertain significance |
| rs148771817 | 7:120,742,980 | C/T | regulatory region variant | — |
| rs13223036 | 7:120,747,308 | T/A | — | — |
| rs798943 | 7:120,758,899 | G/A | intron variant | — |
| rs1296405 | 7:120,759,606 | G/A | intron variant | — |
| rs78333001 | 7:120,761,042 | C/A | — | — |
| rs368245288 | 7:120,764,458 | T/C | — | uncertain significance |
| rs148370748 | 7:120,764,476 | C/T | — | likely benign |
| rs2485416482 | 7:120,764,497 | C/T | — | uncertain significance |
| rs749676033 | 7:120,764,499 | T/A | — | uncertain significance |
| rs200186503 | 7:120,764,515 | A/C | — | uncertain significance |
| rs545698348 | 7:120,765,942 | T/C | — | uncertain significance |
| rs1487802353 | 7:120,767,147 | C/T | — | uncertain significance |
| rs754472602 | 7:120,767,149 | C/G | — | uncertain significance |
| rs2485424024 | 7:120,767,168 | G/C | — | uncertain significance |
| rs138420997 | 7:120,767,194 | C/A | — | uncertain significance |
| rs1381284878 | 7:120,767,249 | G/A | — | uncertain significance |
| rs201639191 | 7:120,768,464 | A/G | — | uncertain significance |
| rs146098402 | 7:120,768,476 | T/C | — | uncertain significance |
| rs772751460 | 7:120,770,218 | C/A | — | uncertain significance |
| rs2485432879 | 7:120,770,222 | A/C | — | uncertain significance |
| rs149346746 | 7:120,770,321 | A/G | — | uncertain significance |
| rs369043917 | 7:120,770,335 | C/T | — | uncertain significance |
| rs755317519 | 7:120,773,912 | C/T | — | uncertain significance |
| rs1401100021 | 7:120,773,928 | T/A | — | uncertain significance |
| rs148690363 | 7:120,773,935 | G/A | — | uncertain significance |
| rs34249834 | 7:120,774,116 | C/A | intron variant | — |
| rs7801723 | 7:120,774,160 | C/T | intron variant | — |
| rs12706318 | 7:120,774,941 | A/G | intron variant | — |
| rs190543052 | 7:120,776,099 | G/T | missense variant | — |
| rs34770628 | 7:120,779,576 | C/T | intron variant | — |
| rs872008 | 7:120,779,990 | G/T | — | — |
| rs884373 | 7:120,780,483 | G/T | intron variant | — |
| rs767858224 | 7:120,780,899 | A/G | — | uncertain significance |
| rs139684091 | 7:120,781,038 | G/C | — | uncertain significance |
| rs2485461946 | 7:120,781,063 | C/T | — | uncertain significance |
| rs138199492 | 7:120,782,078 | T/A | — | benign |
| rs1795918805 | 7:120,782,134 | A/G | — | uncertain significance |
| rs2485465549 | 7:120,782,181 | T/A | — | uncertain significance |
| rs13245690 | 7:120,785,064 | A/G | intron variant | — |
| rs56335989 | 7:120,790,559 | T/C | intron variant | — |
| rs10240772 | 7:120,794,845 | A/G | intron variant | — |
| rs12706319 | 7:120,806,196 | A/C | — | — |
| rs1112810 | 7:120,812,574 | T/C | intron variant | — |
| rs34275932 | 7:120,816,329 | C/G | intron variant | — |
| rs189448695 | 7:120,821,263 | A/G | intron variant | — |
| rs6963115 | 7:120,825,318 | C/A | intron variant | — |
| rs9640799 | 7:120,830,215 | A/G | downstream gene variant | — |
| rs7797976 | 7:120,843,516 | C/T | intron variant | — |
| rs757549740 | 7:120,876,771 | T/C | — | uncertain significance |
| rs2485695256 | 7:120,876,781 | T/C | — | uncertain significance |
| rs373553887 | 7:120,876,789 | C/T | — | uncertain significance |
| rs780572658 | 7:120,876,799 | C/G | — | uncertain significance |
| rs2485695389 | 7:120,876,809 | A/T | — | uncertain significance |
| rs1524506 | 7:120,877,001 | A/T | intron variant | — |
| rs145897714 | 7:120,884,298 | C/T | — | uncertain significance |
| rs1286505445 | 7:120,884,356 | T/G | — | likely benign |
| rs6942652 | 7:120,889,272 | G/T | — | — |
| rs200299025 | 7:120,891,886 | A/G | — | — |
| rs2222543 | 7:120,902,185 | G/A | — | — |
| rs4609139 | 7:120,903,815 | A/T | intron variant | — |
| rs1010372698 | 7:120,906,497 | C/G | — | uncertain significance |
| rs60982266 | 7:120,907,266 | C/A | — | benign |
| rs375914220 | 7:120,907,313 | T/C | — | uncertain significance |
| rs756607568 | 7:120,907,343 | A/G | — | uncertain significance |
| rs2116748189 | 7:120,907,355 | A/G | — | uncertain significance |
| rs141494536 | 7:120,911,388 | A/C | — | likely benign |
| rs781056763 | 7:120,911,394 | A/T | — | uncertain significance |
| rs762096946 | 7:120,911,437 | C/T | — | uncertain significance |
| rs798911 | 7:120,911,462 | A/C | — | benign |
| rs149333699 | 7:120,918,863 | A/G | regulatory region variant | — |
| rs7795061 | 7:120,933,045 | C/T | intron variant | — |
Showing 100 of 102 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.