MFSD6
major facilitator superfamily domain containing 6
Summary
Predicted to enable MHC class I protein binding activity and MHC class I receptor activity. Predicted to be involved in antigen processing and presentation of exogenous peptide antigen via MHC class I. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs374523031 | 2:191,295,544 | G/C | — | — |
| rs2468759484 | 2:191,300,840 | A/G | — | uncertain significance |
| rs73050072 | 2:191,300,916 | T/C | — | benign |
| rs150345541 | 2:191,300,953 | C/T | — | benign |
| rs374826264 | 2:191,301,008 | C/T | — | uncertain significance |
| rs1686174755 | 2:191,301,030 | A/G | — | uncertain significance |
| rs758758860 | 2:191,301,084 | G/A | — | uncertain significance |
| rs199817690 | 2:191,301,242 | A/G | — | uncertain significance |
| rs913751558 | 2:191,301,341 | C/T | — | uncertain significance |
| rs201082615 | 2:191,301,488 | A/T | — | uncertain significance |
| rs1206057963 | 2:191,301,522 | C/T | — | uncertain significance |
| rs142126092 | 2:191,301,549 | C/T | — | uncertain significance |
| rs370513420 | 2:191,301,572 | G/T | — | uncertain significance |
| rs771491282 | 2:191,301,577 | A/C | — | uncertain significance |
| rs113040578 | 2:191,301,640 | C/T | — | benign |
| rs1018680881 | 2:191,301,659 | A/T | — | uncertain significance |
| rs779005349 | 2:191,301,677 | A/G | — | uncertain significance |
| rs149704922 | 2:191,301,700 | G/A | — | benign |
| rs536766738 | 2:191,301,788 | G/A | — | uncertain significance |
| rs765928303 | 2:191,301,861 | A/G | — | uncertain significance |
| rs554501896 | 2:191,301,884 | G/A | — | uncertain significance |
| rs776138868 | 2:191,301,930 | G/A | — | uncertain significance |
| rs2468764690 | 2:191,301,963 | G/C | — | uncertain significance |
| rs767648629 | 2:191,301,971 | G/T | — | uncertain significance |
| rs376329761 | 2:191,301,981 | C/T | — | uncertain significance |
| rs1648695933 | 2:191,301,996 | A/G | — | uncertain significance |
| rs2468765147 | 2:191,302,016 | G/C | — | uncertain significance |
| rs2468765265 | 2:191,302,038 | G/T | — | uncertain significance |
| rs750535885 | 2:191,302,044 | C/T | — | uncertain significance |
| rs2468765918 | 2:191,302,194 | C/T | — | uncertain significance |
| rs2468891013 | 2:191,334,558 | T/G | — | uncertain significance |
| rs79431248 | 2:191,339,523 | G/C | — | — |
| rs201520851 | 2:191,353,442 | C/G | — | uncertain significance |
| rs2468992810 | 2:191,354,524 | T/C | — | uncertain significance |
| rs147604967 | 2:191,362,267 | T/C | — | uncertain significance |
| rs1689774240 | 2:191,362,285 | C/T | — | uncertain significance |
| rs1465452197 | 2:191,362,341 | G/A | — | uncertain significance |
| rs768389713 | 2:191,364,784 | A/G | — | likely benign |
| rs774286665 | 2:191,364,804 | C/A | — | uncertain significance |
| rs758862665 | 2:191,364,867 | C/T | — | uncertain significance |
| rs749919012 | 2:191,364,870 | G/A | — | uncertain significance |
| rs572734082 | 2:191,364,873 | C/A | — | uncertain significance |
| rs778604042 | 2:191,364,880 | G/T | — | uncertain significance |
| rs763412616 | 2:191,364,918 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.