AIFM2
AIF family member 2, ferroptosis suppressor
Summary
This gene encodes a flavoprotein oxidoreductase that binds single stranded DNA and is thought to contribute to apoptosis in the presence of bacterial and viral DNA. The expression of this gene is also found to be induced by tumor suppressor protein p53 in colon cancer cells. [provided by RefSeq, Nov 2010]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs146783519 | 10:71,873,968 | G/A | — | uncertain significance |
| rs145638743 | 10:71,873,987 | G/A | — | uncertain significance |
| rs200384144 | 10:71,874,013 | C/T | — | uncertain significance |
| rs542314841 | 10:71,874,014 | G/A | — | uncertain significance |
| rs142016168 | 10:71,874,085 | C/T | — | uncertain significance |
| rs376374471 | 10:71,874,678 | G/A | — | uncertain significance |
| rs368855181 | 10:71,874,697 | G/C | — | uncertain significance |
| rs149267164 | 10:71,874,726 | G/A | — | uncertain significance |
| rs774471671 | 10:71,874,733 | C/T | — | uncertain significance |
| rs148682063 | 10:71,874,781 | C/T | — | uncertain significance |
| rs145619443 | 10:71,876,389 | C/T | — | uncertain significance |
| rs143261580 | 10:71,876,485 | C/T | — | uncertain significance |
| rs753854619 | 10:71,877,618 | C/T | — | uncertain significance |
| rs147089234 | 10:71,877,619 | G/A | — | uncertain significance |
| rs137970860 | 10:71,877,622 | C/T | — | uncertain significance |
| rs1196426592 | 10:71,880,892 | T/C | — | uncertain significance |
| rs374856767 | 10:71,880,936 | G/A | — | uncertain significance |
| rs766635300 | 10:71,883,228 | T/A | — | uncertain significance |
| rs771696445 | 10:71,883,271 | C/T | — | uncertain significance |
| rs200533003 | 10:71,883,695 | T/C | — | uncertain significance |
| rs754619564 | 10:71,883,716 | A/G | — | uncertain significance |
| rs754745933 | 10:71,883,792 | C/T | — | uncertain significance |
| rs922700901 | 10:71,883,797 | A/G | — | uncertain significance |
| rs1162566060 | 10:71,883,806 | A/G | — | uncertain significance |
| rs372676967 | 10:71,883,815 | G/A | — | uncertain significance |
| rs775593494 | 10:71,883,824 | G/A | — | uncertain significance |
| rs41277978 | 10:71,883,836 | C/A | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.