AIM2
absent in melanoma 2
Summary
AIM2 is a member of the IFI20X /IFI16 family. It plays a putative role in tumorigenic reversion and may control cell proliferation. Interferon-gamma induces expression of AIM2. [provided by RefSeq, Jul 2008]
Known Variants22 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs74689714 | 1:159,032,484 | A/C | — | conflicting classifications of pathogenicity |
| rs753715706 | 1:159,033,331 | A/T | — | uncertain significance |
| rs145779112 | 1:159,033,349 | C/T | — | uncertain significance |
| rs771344708 | 1:159,033,377 | T/C | — | uncertain significance |
| rs376512880 | 1:159,033,386 | C/T | — | uncertain significance |
| rs2525227773 | 1:159,033,392 | T/C | — | likely benign |
| rs34419602 | 1:159,035,721 | A/G | — | benign |
| rs1656070507 | 1:159,035,756 | T/C | — | uncertain significance |
| rs34654901 | 1:159,035,766 | C/A | — | benign |
| rs1305038517 | 1:159,035,827 | G/A | — | uncertain significance |
| rs2525241471 | 1:159,035,884 | C/A | — | uncertain significance |
| rs760089097 | 1:159,035,935 | T/C | — | uncertain significance |
| rs368263314 | 1:159,035,965 | T/C | — | uncertain significance |
| rs768127211 | 1:159,035,968 | G/A | — | uncertain significance |
| rs756118457 | 1:159,035,983 | T/C | — | uncertain significance |
| rs2101967997 | 1:159,036,077 | C/T | — | uncertain significance |
| rs114667580 | 1:159,038,352 | T/A | — | benign |
| rs2525254724 | 1:159,038,405 | C/A | — | uncertain significance |
| rs34479821 | 1:159,043,041 | C/T | — | benign |
| rs1388611876 | 1:159,043,127 | T/C | — | uncertain significance |
| rs1656453919 | 1:159,043,154 | T/C | — | uncertain significance |
| rs855873 | 1:159,047,712 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.