DDIAS
DNA damage induced apoptosis suppressor
Summary
Involved in negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage and regulation of DNA stability. Predicted to be active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs77599934 | 11:82,617,917 | A/G | intron variant | — |
| rs11233371 | 11:82,623,337 | T/C | intron variant | — |
| rs142883872 | 11:82,625,788 | G/A | — | uncertain significance |
| rs2495817162 | 11:82,625,869 | C/G | — | uncertain significance |
| rs1024579965 | 11:82,625,876 | A/G | — | uncertain significance |
| rs775172518 | 11:82,625,883 | G/A | — | uncertain significance |
| rs145120060 | 11:82,641,233 | C/A | — | uncertain significance |
| rs1860954006 | 11:82,641,239 | A/G | — | uncertain significance |
| rs757917726 | 11:82,641,252 | A/G | — | uncertain significance |
| rs201480857 | 11:82,641,264 | C/G | — | uncertain significance |
| rs1860990273 | 11:82,642,781 | A/G | — | uncertain significance |
| rs2495855633 | 11:82,642,818 | C/A | — | uncertain significance |
| rs140644636 | 11:82,642,894 | A/G | — | likely benign |
| rs375366256 | 11:82,642,948 | T/A | — | uncertain significance |
| rs1363982705 | 11:82,643,004 | T/A | — | likely benign |
| rs1260645203 | 11:82,643,017 | G/C | — | uncertain significance |
| rs1213734711 | 11:82,643,041 | G/A | — | uncertain significance |
| rs373346909 | 11:82,643,113 | T/C | — | likely benign |
| rs532135569 | 11:82,643,273 | T/C | — | uncertain significance |
| rs1330831124 | 11:82,643,357 | A/C | — | uncertain significance |
| rs2495859394 | 11:82,643,545 | G/T | — | uncertain significance |
| rs768697292 | 11:82,643,726 | A/C | — | uncertain significance |
| rs2495860463 | 11:82,643,759 | G/A | — | uncertain significance |
| rs1861027523 | 11:82,643,848 | T/A | — | likely benign |
| rs144489743 | 11:82,643,932 | G/C | — | uncertain significance |
| rs145341450 | 11:82,644,078 | G/C | — | uncertain significance |
| rs1415985409 | 11:82,644,350 | T/C | — | uncertain significance |
| rs774695352 | 11:82,644,361 | G/A | — | likely benign |
| rs147036865 | 11:82,644,379 | A/G | — | uncertain significance |
| rs2495863792 | 11:82,644,386 | A/G | — | uncertain significance |
| rs201671760 | 11:82,644,445 | A/G | — | uncertain significance |
| rs773428783 | 11:82,644,523 | G/A | — | uncertain significance |
| rs2495864898 | 11:82,644,590 | A/G | — | uncertain significance |
| rs1480575125 | 11:82,644,608 | G/A | — | uncertain significance |
| rs201151239 | 11:82,644,611 | A/C | — | uncertain significance |
| rs760885843 | 11:82,644,626 | C/T | — | uncertain significance |
| rs2495865339 | 11:82,644,674 | G/C | — | uncertain significance |
| rs149306351 | 11:82,644,709 | A/G | — | likely benign |
| rs377352381 | 11:82,644,841 | C/T | — | uncertain significance |
| rs200675617 | 11:82,644,892 | A/G | — | likely benign |
| rs150700476 | 11:82,645,015 | G/C | — | uncertain significance |
| rs753952402 | 11:82,645,172 | A/G | — | uncertain significance |
| rs1407572913 | 11:82,645,328 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.