DCHS2
dachsous cadherin-related 2
Summary
This gene encodes a large protein that contains many cadherin domains and likely functions in cell adhesion. Genome-wide association studies suggest that this gene may be important in Alzheimer's disease, compressive strength index, and appendicular lean mass. [provided by RefSeq, May 2017]
Known Variants176 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs139235484 | 4:155,155,797 | G/A | — | likely benign |
| rs61746111 | 4:155,155,914 | G/A | — | benign |
| rs7655799 | 4:155,156,207 | A/G | — | benign |
| rs61738813 | 4:155,156,247 | G/A | — | benign |
| rs138106573 | 4:155,156,399 | G/A | — | benign |
| rs61746132 | 4:155,156,412 | G/A | — | benign |
| rs61741046 | 4:155,156,542 | G/A | — | benign |
| rs149548848 | 4:155,156,598 | G/A | — | likely benign |
| rs74491447 | 4:155,156,674 | G/A | — | likely benign |
| rs73857226 | 4:155,156,750 | T/A | — | benign |
| rs61746101 | 4:155,156,875 | T/G | — | benign |
| rs61743677 | 4:155,157,015 | C/T | — | benign |
| rs200042662 | 4:155,157,160 | G/T | — | benign |
| rs114015145 | 4:155,157,404 | C/T | — | benign |
| rs6824133 | 4:155,157,531 | C/T | — | benign |
| rs61746061 | 4:155,157,730 | G/A | — | benign |
| rs111455548 | 4:155,157,871 | A/G | — | benign |
| rs114377700 | 4:155,157,953 | A/G | — | benign |
| rs61741015 | 4:155,157,961 | C/T | — | benign |
| rs111684589 | 4:155,158,090 | A/C | — | benign |
| rs146298768 | 4:155,158,284 | A/C | — | likely benign |
| rs150004475 | 4:155,160,429 | A/G | — | benign |
| rs41280475 | 4:155,161,887 | A/G | — | benign |
| rs200803727 | 4:155,176,790 | G/A | — | benign |
| rs146577159 | 4:155,181,996 | C/T | intron variant | — |
| rs146032523 | 4:155,191,162 | G/A | — | benign |
| rs763710052 | 4:155,191,170 | A/G | — | likely benign |
| rs150202160 | 4:155,219,250 | A/G | synonymous variant | — |
| rs28561984 | 4:155,219,318 | C/G | — | benign |
| rs17031387 | 4:155,219,361 | G/A | — | benign |
| rs17031391 | 4:155,219,373 | A/G | — | benign |
| rs116029479 | 4:155,219,382 | G/C | — | benign |
| rs141467714 | 4:155,219,540 | C/A | — | likely benign |
| rs74321456 | 4:155,219,549 | T/G | — | benign |
| rs17031394 | 4:155,219,662 | G/C | — | benign |
| rs114469698 | 4:155,219,788 | C/A | — | benign |
| rs115999956 | 4:155,225,951 | G/A | — | benign |
| rs28622098 | 4:155,226,021 | C/T | — | benign |
| rs1043043410 | 4:155,241,522 | G/A | — | likely benign |
| rs1736008684 | 4:155,241,523 | C/A | — | likely benign |
| rs11935573 | 4:155,241,572 | G/A | — | benign |
| rs56277131 | 4:155,241,674 | G/A | — | benign |
| rs79535970 | 4:155,241,735 | C/T | — | benign |
| rs146199349 | 4:155,241,937 | G/A | — | likely benign |
| rs112514539 | 4:155,242,011 | G/A | — | benign |
| rs193920995 | 4:155,242,176 | C/T | — | uncertain significance |
| rs62331873 | 4:155,242,383 | C/T | — | benign |
| rs13109747 | 4:155,243,573 | C/T | — | benign |
| rs75387086 | 4:155,243,603 | A/G | — | benign |
| rs1352714 | 4:155,243,604 | C/T | — | benign |
| rs142864637 | 4:155,243,612 | G/A | — | benign |
| rs74430037 | 4:155,244,462 | C/T | — | benign |
| rs12500437 | 4:155,244,475 | T/G | — | benign |
| rs111557030 | 4:155,249,289 | G/A | — | likely benign |
| rs760885306 | 4:155,249,344 | C/T | — | uncertain significance |
| rs79295524 | 4:155,250,701 | G/C | — | benign |
| rs368868441 | 4:155,250,748 | A/G | — | uncertain significance |
| rs7666283 | 4:155,250,749 | C/T | — | benign |
| rs557854971 | 4:155,250,757 | G/A | — | likely benign |
| rs202003400 | 4:155,250,785 | C/T | — | uncertain significance |
| rs34249493 | 4:155,250,786 | A/G | — | benign |
| rs539253714 | 4:155,250,787 | C/A | — | uncertain significance |
| rs368981576 | 4:155,250,788 | G/A | — | uncertain significance |
| rs750022860 | 4:155,250,803 | C/T | — | uncertain significance |
| rs1385723957 | 4:155,250,845 | C/T | — | uncertain significance |
| rs7672337 | 4:155,251,610 | A/G | intron variant | — |
| rs779194391 | 4:155,252,758 | G/A | — | uncertain significance |
| rs141064025 | 4:155,253,684 | G/A | — | benign |
| rs151280397 | 4:155,253,759 | C/T | — | uncertain significance |
| rs1375718725 | 4:155,253,810 | C/T | — | uncertain significance |
| rs2530198465 | 4:155,253,828 | T/C | — | uncertain significance |
| rs2530198576 | 4:155,253,848 | T/G | — | uncertain significance |
| rs767023019 | 4:155,253,881 | A/G | — | uncertain significance |
| rs376143824 | 4:155,253,926 | C/A | — | uncertain significance |
| rs1736600493 | 4:155,253,951 | G/A | — | uncertain significance |
| rs112836372 | 4:155,253,964 | C/T | — | likely benign |
| rs1407281586 | 4:155,254,002 | G/C | — | uncertain significance |
| rs2530199552 | 4:155,254,004 | G/A | — | uncertain significance |
| rs2530199708 | 4:155,254,031 | G/A | — | uncertain significance |
| rs777577872 | 4:155,254,034 | T/C | — | uncertain significance |
| rs113845841 | 4:155,254,051 | C/T | — | likely benign |
| rs572981878 | 4:155,254,089 | C/T | — | uncertain significance |
| rs755977541 | 4:155,254,121 | G/A | — | uncertain significance |
| rs1350555668 | 4:155,254,136 | T/G | — | uncertain significance |
| rs1323078493 | 4:155,254,140 | C/G | — | uncertain significance |
| rs74422312 | 4:155,254,146 | C/A | — | likely benign |
| rs149462928 | 4:155,254,155 | G/A | — | benign |
| rs143911538 | 4:155,254,156 | C/T | — | benign |
| rs762952228 | 4:155,254,176 | G/T | — | uncertain significance |
| rs767417856 | 4:155,254,177 | A/T | — | uncertain significance |
| rs567129224 | 4:155,254,235 | C/G | — | uncertain significance |
| rs183199511 | 4:155,254,268 | G/A | — | uncertain significance |
| rs765925742 | 4:155,254,298 | G/T | — | likely benign |
| rs139082640 | 4:155,254,355 | C/A | — | uncertain significance |
| rs966529960 | 4:155,254,398 | T/G | — | uncertain significance |
| rs1267917142 | 4:155,254,424 | A/G | — | uncertain significance |
| rs72966167 | 4:155,254,428 | C/T | — | benign |
| rs2530202798 | 4:155,254,506 | C/T | — | uncertain significance |
| rs76121430 | 4:155,254,512 | C/A | — | benign |
| rs112889386 | 4:155,254,523 | A/G | — | benign |
Showing 100 of 176 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.