SLC2A6
solute carrier family 2 member 6
Summary
Hexose transport into mammalian cells is catalyzed by a family of membrane proteins, including SLC2A6, that contain 12 transmembrane domains and a number of critical conserved residues.[supplied by OMIM, Jul 2002]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4962054 | 9:136,336,933 | G/A | downstream gene variant | — |
| rs781974590 | 9:136,337,201 | C/T | — | uncertain significance |
| rs2490689981 | 9:136,338,229 | C/T | — | uncertain significance |
| rs781946360 | 9:136,338,256 | C/T | — | uncertain significance |
| rs144991293 | 9:136,338,306 | C/T | — | uncertain significance |
| rs782667357 | 9:136,338,334 | T/C | — | uncertain significance |
| rs782204608 | 9:136,338,354 | C/T | — | uncertain significance |
| rs1554802295 | 9:136,338,590 | G/T | — | uncertain significance |
| rs374710721 | 9:136,338,623 | G/T | — | uncertain significance |
| rs142346579 | 9:136,338,627 | C/T | — | uncertain significance |
| rs782314046 | 9:136,338,659 | A/G | — | uncertain significance |
| rs201147280 | 9:136,339,108 | C/T | — | uncertain significance |
| rs782337904 | 9:136,339,150 | C/T | — | uncertain significance |
| rs782694774 | 9:136,339,177 | C/T | — | uncertain significance |
| rs782777517 | 9:136,340,199 | G/A | — | uncertain significance |
| rs367744627 | 9:136,340,228 | C/T | — | uncertain significance |
| rs28393320 | 9:136,340,436 | T/C | downstream gene variant | — |
| rs115835881 | 9:136,340,534 | G/A | — | benign |
| rs201897933 | 9:136,340,551 | C/G | — | uncertain significance |
| rs115761379 | 9:136,340,577 | G/T | — | uncertain significance |
| rs376983675 | 9:136,340,583 | C/G | — | uncertain significance |
| rs370961911 | 9:136,340,643 | G/A | — | uncertain significance |
| rs372800038 | 9:136,340,715 | C/T | — | uncertain significance |
| rs146427075 | 9:136,341,365 | C/T | — | uncertain significance |
| rs932317336 | 9:136,342,167 | G/C | — | uncertain significance |
| rs1165263123 | 9:136,342,207 | C/T | — | uncertain significance |
| rs782298579 | 9:136,342,229 | G/T | — | uncertain significance |
| rs375116279 | 9:136,342,239 | G/A | — | uncertain significance |
| rs748053482 | 9:136,342,321 | T/C | — | uncertain significance |
| rs1554803670 | 9:136,342,336 | C/T | — | uncertain significance |
| rs35885350 | 9:136,343,408 | G/A | — | benign |
| rs370358917 | 9:136,343,452 | G/A | — | uncertain significance |
| rs782296929 | 9:136,343,492 | G/C | — | uncertain significance |
| rs139030106 | 9:136,343,516 | A/G | — | uncertain significance |
| rs115492351 | 9:136,343,524 | T/C | — | benign |
| rs2490734269 | 9:136,344,127 | T/C | — | uncertain significance |
| rs201285256 | 9:136,344,142 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.