SLC35F1
solute carrier family 35 member F1
Summary
Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Located in synaptic vesicle membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs756765575 | 6:118,228,895 | C/G | — | uncertain significance |
| rs772014633 | 6:118,228,899 | C/G | — | uncertain significance |
| rs949586549 | 6:118,228,933 | C/T | — | uncertain significance |
| rs979887993 | 6:118,228,945 | C/G | — | uncertain significance |
| rs2482328843 | 6:118,229,023 | G/A | — | uncertain significance |
| rs1054395950 | 6:118,229,042 | G/T | — | uncertain significance |
| rs11153718 | 6:118,372,057 | G/A | — | association |
| rs2482367616 | 6:118,475,675 | A/G | — | uncertain significance |
| rs1413846 | 6:118,527,888 | A/G | intron variant | — |
| rs1413845 | 6:118,528,018 | C/A | — | — |
| rs457162 | 6:118,535,983 | A/T | intron variant | — |
| rs773864511 | 6:118,556,699 | G/C | — | uncertain significance |
| rs745950537 | 6:118,556,702 | G/A | — | uncertain significance |
| rs17079881 | 6:118,566,187 | A/G | intron variant | — |
| rs9372498 | 6:118,572,486 | T/A | intron variant | — |
| rs281868 | 6:118,574,061 | G/A | intron variant | — |
| rs89107 | 6:118,578,043 | G/A | intron variant | — |
| rs62421489 | 6:118,601,980 | G/A | intron variant | — |
| rs201823028 | 6:118,606,358 | G/A | — | uncertain significance |
| rs1304499333 | 6:118,606,377 | T/G | — | uncertain significance |
| rs756395092 | 6:118,606,395 | T/G | — | uncertain significance |
| rs76108627 | 6:118,606,403 | G/A | — | uncertain significance |
| rs1630266 | 6:118,612,943 | G/A | intron variant | — |
| rs166881 | 6:118,618,981 | T/C | intron variant | — |
| rs371673898 | 6:118,635,299 | C/T | — | uncertain significance |
| rs138680595 | 6:118,635,300 | G/A | — | uncertain significance |
| rs141802559 | 6:118,635,315 | C/A | — | uncertain significance |
| rs41291934 | 6:118,635,331 | G/A | — | benign |
| rs2533571331 | 6:118,635,380 | G/C | — | uncertain significance |
| rs381999 | 6:118,636,793 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.