SLC22A25
solute carrier family 22 member 25
Summary
Predicted to enable transmembrane transporter activity. Predicted to be involved in organic anion transport. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs760041363 | 11:62,931,312 | C/T | — | uncertain significance |
| rs141450282 | 11:62,931,369 | A/G | — | likely benign |
| rs1171741106 | 11:62,931,384 | C/G | — | uncertain significance |
| rs1365263685 | 11:62,931,411 | A/G | — | uncertain significance |
| rs2087588950 | 11:62,931,423 | A/G | — | uncertain significance |
| rs1032791207 | 11:62,931,438 | T/C | — | uncertain significance |
| rs2539079275 | 11:62,931,471 | C/T | — | uncertain significance |
| rs1238485866 | 11:62,931,501 | C/T | — | uncertain significance |
| rs976059004 | 11:62,931,517 | A/G | — | uncertain significance |
| rs745995908 | 11:62,931,541 | T/G | — | likely benign |
| rs2087613365 | 11:62,932,005 | T/C | — | likely benign |
| rs775776820 | 11:62,933,545 | C/T | — | uncertain significance |
| rs941361673 | 11:62,933,570 | G/T | — | uncertain significance |
| rs201794592 | 11:62,933,574 | C/A | — | uncertain significance |
| rs201276215 | 11:62,933,575 | T/G | — | uncertain significance |
| rs777351917 | 11:62,933,665 | A/G | — | uncertain significance |
| rs370163289 | 11:62,933,689 | A/G | — | uncertain significance |
| rs763090125 | 11:62,933,708 | A/C | — | uncertain significance |
| rs908753725 | 11:62,948,151 | A/G | — | uncertain significance |
| rs201321403 | 11:62,948,219 | A/G | — | uncertain significance |
| rs770061534 | 11:62,948,230 | C/A | — | uncertain significance |
| rs763396567 | 11:62,948,236 | G/T | — | likely benign |
| rs892906840 | 11:62,951,171 | T/C | — | uncertain significance |
| rs1251128669 | 11:62,951,286 | C/G | — | uncertain significance |
| rs189314066 | 11:62,963,123 | A/G | intron variant | — |
| rs2089739030 | 11:62,984,827 | C/G | — | uncertain significance |
| rs199866396 | 11:62,985,065 | T/C | — | uncertain significance |
| rs762029744 | 11:62,985,107 | G/A | — | uncertain significance |
| rs117914773 | 11:62,985,123 | G/A | — | likely benign |
| rs200325838 | 11:62,985,145 | G/A | — | uncertain significance |
| rs770798148 | 11:62,985,154 | C/T | — | likely benign |
| rs201370159 | 11:62,985,164 | C/T | — | uncertain significance |
| rs563995072 | 11:62,985,173 | G/A | — | likely benign |
| rs117070489 | 11:62,987,766 | C/T | intron variant | — |
| rs144340167 | 11:62,995,925 | A/G | — | likely benign |
| rs377364307 | 11:62,995,934 | T/C | — | uncertain significance |
| rs1783657 | 11:62,996,038 | T/C | — | benign |
| rs74759635 | 11:62,996,682 | G/A | — | — |
| rs142427382 | 11:62,996,823 | A/G | — | uncertain significance |
| rs145812369 | 11:62,996,836 | T/C | — | likely benign |
| rs773392931 | 11:62,996,841 | T/C | — | uncertain significance |
| rs143454012 | 11:62,996,865 | T/A | — | likely benign |
| rs1020892248 | 11:62,996,934 | G/A | — | uncertain significance |
| rs150691466 | 11:62,996,948 | G/T | — | likely benign |
| rs753160640 | 11:62,996,965 | G/C | — | uncertain significance |
| rs764453197 | 11:62,996,982 | C/T | — | uncertain significance |
| rs34499840 | 11:62,997,031 | A/G | — | likely benign |
| rs150920552 | 11:62,997,041 | G/A | synonymous variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.