SLC35F3
solute carrier family 35 member F3
Summary
Involved in thiamine transport. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs142850003 | 1:234,040,848 | G/A | — | uncertain significance |
| rs145835583 | 1:234,041,416 | C/A | — | uncertain significance |
| rs374192783 | 1:234,098,265 | C/G | — | — |
| rs532298969 | 1:234,158,787 | G/A | — | — |
| rs535673445 | 1:234,213,523 | G/A | — | — |
| rs746872593 | 1:234,367,184 | C/G | — | uncertain significance |
| rs2102950752 | 1:234,367,238 | C/T | — | uncertain significance |
| rs780024830 | 1:234,367,243 | C/T | — | uncertain significance |
| rs1179264708 | 1:234,367,247 | G/A | — | uncertain significance |
| rs34032258 | 1:234,367,264 | C/G | missense variant | benign |
| rs771538452 | 1:234,367,276 | A/G | — | uncertain significance |
| rs200834507 | 1:234,367,294 | G/T | — | uncertain significance |
| rs1667376316 | 1:234,367,312 | G/C | — | uncertain significance |
| rs778098021 | 1:234,367,403 | A/G | — | uncertain significance |
| rs746025325 | 1:234,367,448 | G/T | — | uncertain significance |
| rs573421908 | 1:234,420,503 | G/A | — | — |
| rs6657486 | 1:234,452,338 | G/A | — | benign |
| rs754200916 | 1:234,452,396 | G/C | — | uncertain significance |
| rs758151372 | 1:234,454,528 | A/G | — | uncertain significance |
| rs955692073 | 1:234,454,599 | A/G | — | likely benign |
| rs753316921 | 1:234,454,677 | G/T | — | uncertain significance |
| rs539243199 | 1:234,455,853 | T/C | — | uncertain significance |
| rs377116741 | 1:234,455,876 | G/A | — | uncertain significance |
| rs776200248 | 1:234,458,776 | G/C | — | uncertain significance |
| rs200614672 | 1:234,458,787 | A/G | — | uncertain significance |
| rs34618966 | 1:234,458,854 | G/A | — | benign |
| rs2526860802 | 1:234,458,924 | G/A | — | uncertain significance |
| rs754124985 | 1:234,458,977 | C/T | — | likely benign |
| rs765371968 | 1:234,458,981 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.