SFXN2
sideroflexin 2
Summary
Predicted to enable transmembrane transporter activity. Involved in mitochondrial transmembrane transport. Located in mitochondrial outer membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7905481 | 10:104,476,292 | T/C | upstream gene variant | — |
| rs11191379 | 10:104,482,330 | C/G | — | — |
| rs12259058 | 10:104,484,799 | A/T | — | — |
| rs1333293653 | 10:104,486,427 | G/A | — | uncertain significance |
| rs374128920 | 10:104,486,445 | C/T | — | likely benign |
| rs200012623 | 10:104,486,485 | C/T | — | uncertain significance |
| rs201068739 | 10:104,486,493 | C/T | — | uncertain significance |
| rs201929596 | 10:104,486,494 | G/A | — | uncertain significance |
| rs140197433 | 10:104,486,515 | G/A | — | likely benign |
| rs776068305 | 10:104,486,812 | C/A | — | uncertain significance |
| rs2493049857 | 10:104,486,816 | C/A | — | uncertain significance |
| rs144952394 | 10:104,486,823 | G/A | — | uncertain significance |
| rs149056754 | 10:104,486,826 | A/G | — | uncertain significance |
| rs754171008 | 10:104,486,877 | G/A | — | uncertain significance |
| rs779086845 | 10:104,486,890 | C/T | — | uncertain significance |
| rs747372762 | 10:104,486,896 | T/C | — | uncertain significance |
| rs771346744 | 10:104,486,899 | T/G | — | uncertain significance |
| rs2902548 | 10:104,487,382 | C/G | — | — |
| rs1161367189 | 10:104,488,256 | A/G | — | uncertain significance |
| rs767631605 | 10:104,489,128 | G/T | — | uncertain significance |
| rs368893496 | 10:104,489,484 | C/T | — | uncertain significance |
| rs765737805 | 10:104,489,487 | C/T | — | uncertain significance |
| rs368748485 | 10:104,489,490 | C/T | — | uncertain significance |
| rs749839106 | 10:104,489,502 | G/A | — | uncertain significance |
| rs376492604 | 10:104,489,519 | G/A | — | uncertain significance |
| rs202072523 | 10:104,489,532 | C/T | — | uncertain significance |
| rs143559053 | 10:104,489,559 | G/A | — | uncertain significance |
| rs113903951 | 10:104,493,353 | G/A | — | uncertain significance |
| rs573625364 | 10:104,495,638 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.