ADAMTSL5
ADAMTS like 5
Summary
Enables heparin binding activity and microfibril binding activity. Predicted to be involved in extracellular matrix organization. Located in extracellular region and microfibril. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2512819947 | 19:1,506,019 | C/T | — | likely benign |
| rs144153954 | 19:1,506,031 | G/A | — | likely benign |
| rs747820135 | 19:1,506,085 | C/T | — | uncertain significance |
| rs141903537 | 19:1,506,214 | G/C | — | uncertain significance |
| rs200370374 | 19:1,506,228 | G/A | — | uncertain significance |
| rs778633341 | 19:1,506,256 | G/A | — | uncertain significance |
| rs201754237 | 19:1,506,268 | G/A | — | uncertain significance |
| rs763578743 | 19:1,506,307 | C/A | — | uncertain significance |
| rs746736830 | 19:1,506,601 | C/T | — | uncertain significance |
| rs543863194 | 19:1,506,743 | G/A | — | uncertain significance |
| rs1317084842 | 19:1,506,777 | G/C | — | uncertain significance |
| rs753752128 | 19:1,506,783 | C/T | — | uncertain significance |
| rs777151542 | 19:1,506,806 | C/T | — | uncertain significance |
| rs748641040 | 19:1,506,807 | G/A | — | uncertain significance |
| rs200191805 | 19:1,506,821 | C/A | — | uncertain significance |
| rs760330533 | 19:1,506,848 | C/G | — | uncertain significance |
| rs1216820169 | 19:1,506,849 | G/A | — | uncertain significance |
| rs1034922927 | 19:1,506,875 | C/T | — | likely benign |
| rs753793260 | 19:1,506,876 | G/A | — | uncertain significance |
| rs970555164 | 19:1,506,897 | C/T | — | uncertain significance |
| rs757244835 | 19:1,506,912 | G/C | — | uncertain significance |
| rs984196012 | 19:1,506,918 | G/T | — | uncertain significance |
| rs762922679 | 19:1,507,305 | C/T | — | uncertain significance |
| rs370999410 | 19:1,507,327 | C/T | — | uncertain significance |
| rs2512829437 | 19:1,507,380 | T/C | — | uncertain significance |
| rs141123035 | 19:1,507,392 | C/T | — | uncertain significance |
| rs375519545 | 19:1,507,397 | C/G | — | uncertain significance |
| rs561850127 | 19:1,507,574 | T/C | — | uncertain significance |
| rs769337588 | 19:1,508,000 | C/T | — | uncertain significance |
| rs1346168628 | 19:1,508,078 | C/A | — | uncertain significance |
| rs1328407064 | 19:1,508,480 | G/A | — | uncertain significance |
| rs2512838942 | 19:1,508,510 | C/T | — | uncertain significance |
| rs187957632 | 19:1,508,592 | G/A | coding sequence variant | — |
| rs145681719 | 19:1,510,199 | C/T | — | likely benign |
| rs776983836 | 19:1,510,200 | G/A | — | uncertain significance |
| rs750379187 | 19:1,510,378 | A/T | — | uncertain significance |
| rs368654852 | 19:1,510,390 | C/T | — | uncertain significance |
| rs149832091 | 19:1,510,410 | G/A | — | likely benign |
| rs1041888264 | 19:1,510,639 | G/A | — | uncertain significance |
| rs1024924636 | 19:1,510,650 | C/T | — | uncertain significance |
| rs771316224 | 19:1,510,651 | G/A | — | uncertain significance |
| rs1247502734 | 19:1,510,656 | C/T | — | uncertain significance |
| rs200872673 | 19:1,510,671 | C/T | — | uncertain significance |
| rs1028304898 | 19:1,510,672 | G/A | — | uncertain significance |
| rs550092054 | 19:1,510,692 | C/T | — | uncertain significance |
| rs568666000 | 19:1,510,720 | C/T | — | uncertain significance |
| rs769412213 | 19:1,510,854 | A/G | — | uncertain significance |
| rs1027084023 | 19:1,510,855 | C/A | — | uncertain significance |
| rs1376521248 | 19:1,510,930 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.