ADAMTSL3
ADAMTS like 3
Summary
Predicted to be involved in extracellular matrix organization. Located in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants248 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2730080 | 15:84,324,441 | G/A | — | benign |
| rs181910603 | 15:84,324,526 | A/T | — | uncertain significance |
| rs147914990 | 15:84,324,527 | C/T | — | uncertain significance |
| rs1347296591 | 15:84,324,540 | G/T | — | uncertain significance |
| rs763452372 | 15:84,324,571 | C/T | — | uncertain significance |
| rs757391316 | 15:84,324,581 | A/T | — | uncertain significance |
| rs12148469 | 15:84,330,653 | A/G | — | — |
| rs147726586 | 15:84,338,251 | G/A | intron variant | — |
| rs11639223 | 15:84,372,928 | G/A | — | benign |
| rs200800949 | 15:84,373,157 | C/A | — | likely benign |
| rs890309 | 15:84,373,370 | G/A | — | benign |
| rs1544876 | 15:84,375,801 | T/C | — | — |
| rs367959773 | 15:84,383,616 | C/A | — | — |
| rs10152300 | 15:84,392,907 | G/A | intron variant | — |
| rs7182216 | 15:84,422,506 | C/T | — | — |
| rs56226101 | 15:84,426,284 | C/T | intron variant | — |
| rs11856314 | 15:84,435,531 | C/T | regulatory region variant | — |
| rs72746925 | 15:84,440,251 | C/T | intron variant | — |
| rs75442575 | 15:84,442,272 | T/C | — | benign |
| rs2548731543 | 15:84,442,297 | A/G | — | uncertain significance |
| rs62025779 | 15:84,447,836 | C/T | intron variant | — |
| rs56711701 | 15:84,454,829 | A/G | intron variant | — |
| rs77510589 | 15:84,461,862 | C/G | intron variant | — |
| rs531894480 | 15:84,464,006 | A/G | — | — |
| rs536785166 | 15:84,466,320 | T/C | — | — |
| rs4843158 | 15:84,471,636 | G/C | intron variant | — |
| rs2548818934 | 15:84,473,159 | T/C | — | uncertain significance |
| rs11856213 | 15:84,473,163 | T/C | — | benign |
| rs28504011 | 15:84,473,505 | A/G | — | benign |
| rs7179507 | 15:84,473,531 | G/A | — | benign |
| rs76872043 | 15:84,474,318 | A/T | intron variant | — |
| rs774284803 | 15:84,483,728 | G/A | — | — |
| rs113816378 | 15:84,488,033 | A/C | intron variant | — |
| rs4583200 | 15:84,488,529 | T/C | — | benign |
| rs142393908 | 15:84,488,577 | T/A | — | uncertain significance |
| rs376774419 | 15:84,488,579 | C/T | — | uncertain significance |
| rs4483821 | 15:84,488,636 | A/G | — | benign |
| rs760104348 | 15:84,488,657 | G/A | — | uncertain significance |
| rs201787136 | 15:84,488,762 | C/T | — | uncertain significance |
| rs4583201 | 15:84,489,049 | C/G | — | benign |
| rs11259919 | 15:84,489,802 | A/G | downstream gene variant | — |
| rs6602994 | 15:84,490,757 | T/C | downstream gene variant | — |
| rs376854269 | 15:84,491,203 | A/G | — | — |
| rs9888644 | 15:84,498,332 | G/A | upstream gene variant | — |
| rs4620919 | 15:84,498,945 | C/G | intron variant | — |
| rs7164782 | 15:84,502,199 | C/T | intron variant | — |
| rs12443111 | 15:84,504,479 | A/G | intron variant | — |
| rs35104757 | 15:84,506,570 | A/G | — | benign |
| rs61387269 | 15:84,506,757 | C/A | — | benign |
| rs372374918 | 15:84,506,857 | G/C | — | uncertain significance |
| rs140705133 | 15:84,506,872 | A/G | — | likely benign |
| rs745534521 | 15:84,506,907 | G/A | — | uncertain significance |
| rs2548207096 | 15:84,506,928 | G/T | — | uncertain significance |
| rs12901128 | 15:84,507,075 | C/T | — | benign |
| rs73439446 | 15:84,507,188 | G/A | — | benign |
| rs6602997 | 15:84,521,398 | C/T | intron variant | — |
| rs1383484 | 15:84,522,755 | C/T | intron variant | — |
| rs112269587 | 15:84,527,323 | C/T | — | benign |
| rs113038464 | 15:84,527,364 | A/G | — | benign |
| rs149499512 | 15:84,527,509 | C/G | — | benign |
| rs149710156 | 15:84,527,554 | G/A | — | uncertain significance |
| rs12916455 | 15:84,530,914 | C/A | — | — |
| rs58994367 | 15:84,531,499 | A/G | intron variant | — |
| rs143253231 | 15:84,531,695 | G/A | intron variant | — |
| rs55839613 | 15:84,539,255 | T/C | — | benign |
| rs56159777 | 15:84,539,279 | A/G | — | benign |
| rs4842919 | 15:84,539,420 | G/T | — | benign |
| rs4842920 | 15:84,539,424 | G/T | — | benign |
| rs17158590 | 15:84,539,476 | C/T | — | benign |
| rs549219584 | 15:84,539,557 | T/C | — | uncertain significance |
| rs4144691 | 15:84,539,619 | C/G | — | benign |
| rs759345225 | 15:84,539,673 | A/G | — | uncertain significance |
| rs56100529 | 15:84,542,945 | A/T | — | — |
| rs1812707 | 15:84,547,222 | C/A | — | — |
| rs62025854 | 15:84,552,515 | G/A | — | — |
| rs12900412 | 15:84,553,066 | G/T | — | — |
| rs10220741 | 15:84,553,558 | G/A | — | benign |
| rs12907220 | 15:84,553,623 | T/A | — | benign |
| rs74024592 | 15:84,553,642 | G/A | — | benign |
| rs532624658 | 15:84,553,903 | G/C | — | uncertain significance |
| rs138562816 | 15:84,553,953 | C/T | — | uncertain significance |
| rs112182320 | 15:84,554,012 | A/G | — | benign |
| rs8028931 | 15:84,554,018 | G/C | — | benign |
| rs17158579 | 15:84,554,117 | A/G | — | benign |
| rs76457699 | 15:84,554,201 | A/C | — | benign |
| rs8030566 | 15:84,554,276 | C/A | — | benign |
| rs12591488 | 15:84,558,653 | A/G | — | benign |
| rs28705374 | 15:84,558,676 | A/G | — | benign |
| rs12592484 | 15:84,558,701 | C/T | — | benign |
| rs17158548 | 15:84,558,808 | A/C | — | benign |
| rs775968227 | 15:84,558,887 | G/A | — | uncertain significance |
| rs9329360 | 15:84,560,382 | G/A | — | benign |
| rs57548773 | 15:84,560,716 | C/T | intron variant | — |
| rs768526147 | 15:84,561,626 | A/G | — | uncertain significance |
| rs899927 | 15:84,561,879 | C/T | — | benign |
| rs74024600 | 15:84,566,393 | G/A | — | benign |
| rs7162129 | 15:84,566,444 | T/C | — | benign |
| rs78494571 | 15:84,566,528 | G/C | — | benign |
| rs11259927 | 15:84,566,544 | C/T | — | benign |
| rs141028283 | 15:84,566,644 | G/A | — | uncertain significance |
Showing 100 of 248 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.