SMC2
structural maintenance of chromosomes 2
Summary
Predicted to enable chromatin binding activity. Involved in mitotic chromosome condensation and positive regulation of chromosome condensation. Located in condensed chromosome; cytoplasm; and nuclear lumen. Part of condensin complex. Implicated in colon adenocarcinoma. Biomarker of colorectal cancer. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants79 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3818626 | 9:106,856,633 | C/T | regulatory region variant | — |
| rs4742903 | 9:106,856,793 | G/T | — | — |
| rs1349170852 | 9:106,857,715 | G/A | — | uncertain significance |
| rs1467090794 | 9:106,857,748 | A/G | — | uncertain significance |
| rs3739737 | 9:106,858,192 | A/G | upstream gene variant | — |
| rs755444333 | 9:106,858,553 | A/C | — | uncertain significance |
| rs61755310 | 9:106,860,779 | A/C | — | likely benign |
| rs182149326 | 9:106,862,388 | A/G | — | uncertain significance |
| rs140049238 | 9:106,862,428 | A/G | — | uncertain significance |
| rs200540431 | 9:106,862,483 | C/T | — | uncertain significance |
| rs567910817 | 9:106,864,242 | A/G | — | uncertain significance |
| rs747631183 | 9:106,864,248 | C/G | — | uncertain significance |
| rs1225165289 | 9:106,864,298 | C/T | — | uncertain significance |
| rs1831192568 | 9:106,864,310 | G/T | — | uncertain significance |
| rs2131319286 | 9:106,864,324 | G/T | — | uncertain significance |
| rs767457806 | 9:106,864,331 | G/A | — | uncertain significance |
| rs148946777 | 9:106,864,347 | G/A | — | uncertain significance |
| rs1564072726 | 9:106,864,407 | C/T | — | uncertain significance |
| rs61755103 | 9:106,864,433 | C/T | — | benign |
| rs2537695322 | 9:106,864,708 | A/C | — | uncertain significance |
| rs761107909 | 9:106,864,723 | C/T | — | uncertain significance |
| rs199917130 | 9:106,864,780 | G/A | — | uncertain significance |
| rs138115955 | 9:106,864,807 | G/A | — | benign |
| rs7859034 | 9:106,865,692 | G/T | intron variant | — |
| rs34711584 | 9:106,873,948 | T/C | — | benign |
| rs564322861 | 9:106,873,950 | C/T | — | uncertain significance |
| rs760655816 | 9:106,873,994 | G/T | — | uncertain significance |
| rs149471302 | 9:106,874,040 | G/T | — | uncertain significance |
| rs144046688 | 9:106,874,046 | T/C | — | uncertain significance |
| rs1401714427 | 9:106,874,056 | T/G | — | uncertain significance |
| rs564129335 | 9:106,875,613 | A/G | — | uncertain significance |
| rs745491224 | 9:106,875,624 | C/A | — | uncertain significance |
| rs765098627 | 9:106,875,663 | G/A | — | uncertain significance |
| rs77050953 | 9:106,875,751 | A/T | — | uncertain significance |
| rs776518199 | 9:106,876,275 | G/A | — | uncertain significance |
| rs780909705 | 9:106,876,322 | G/A | — | uncertain significance |
| rs370550727 | 9:106,876,350 | G/A | — | likely benign |
| rs370728212 | 9:106,877,046 | C/A | — | uncertain significance |
| rs1832894310 | 9:106,877,061 | T/C | — | uncertain significance |
| rs1833096430 | 9:106,878,514 | C/G | — | uncertain significance |
| rs375330343 | 9:106,878,532 | A/G | — | uncertain significance |
| rs2537810733 | 9:106,878,535 | A/G | — | uncertain significance |
| rs988464594 | 9:106,878,561 | A/C | — | uncertain significance |
| rs773792221 | 9:106,880,467 | G/C | — | uncertain significance |
| rs76421718 | 9:106,880,515 | G/T | — | benign |
| rs1310755491 | 9:106,880,608 | G/A | — | uncertain significance |
| rs754501045 | 9:106,882,356 | A/G | — | uncertain significance |
| rs149999543 | 9:106,882,398 | G/A | — | likely benign |
| rs902192890 | 9:106,882,421 | G/A | — | uncertain significance |
| rs751204383 | 9:106,882,433 | A/G | — | uncertain significance |
| rs781384156 | 9:106,885,394 | G/A | — | uncertain significance |
| rs1473334121 | 9:106,885,481 | A/G | — | uncertain significance |
| rs2537868725 | 9:106,885,496 | C/T | — | uncertain significance |
| rs376788348 | 9:106,887,301 | G/A | — | uncertain significance |
| rs2537883840 | 9:106,887,342 | A/C | — | uncertain significance |
| rs2537884329 | 9:106,887,379 | A/C | — | uncertain significance |
| rs1432383562 | 9:106,888,958 | A/G | — | uncertain significance |
| rs781366175 | 9:106,888,980 | A/G | — | uncertain significance |
| rs753121778 | 9:106,888,982 | C/A | — | uncertain significance |
| rs760538345 | 9:106,889,019 | A/G | — | uncertain significance |
| rs11554260 | 9:106,889,571 | C/T | — | likely benign |
| rs764390870 | 9:106,889,604 | A/G | — | uncertain significance |
| rs1564109280 | 9:106,889,651 | G/A | — | uncertain significance |
| rs1461374127 | 9:106,889,666 | C/A | — | uncertain significance |
| rs1392989465 | 9:106,889,672 | G/A | — | uncertain significance |
| rs370655070 | 9:106,889,713 | C/A | — | uncertain significance |
| rs1834436764 | 9:106,889,734 | A/C | — | uncertain significance |
| rs777188494 | 9:106,889,735 | C/T | — | uncertain significance |
| rs1022475090 | 9:106,891,944 | G/C | — | uncertain significance |
| rs564171583 | 9:106,891,948 | A/G | — | uncertain significance |
| rs1430479168 | 9:106,894,303 | T/A | — | uncertain significance |
| rs2537947713 | 9:106,894,383 | G/T | — | uncertain significance |
| rs113443856 | 9:106,896,738 | G/A | — | uncertain significance |
| rs1334176020 | 9:106,896,744 | A/G | — | uncertain significance |
| rs1226145038 | 9:106,896,750 | A/G | — | uncertain significance |
| rs372796365 | 9:106,896,759 | C/T | — | uncertain significance |
| rs749136526 | 9:106,896,762 | C/T | — | uncertain significance |
| rs61741732 | 9:106,896,799 | A/G | — | benign |
| rs1407668934 | 9:106,896,814 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.