SLC30A3
solute carrier family 30 member 3
Summary
Enables zinc ion transmembrane transporter activity. Involved in zinc ion import into lysosome. Located in late endosome and synaptic vesicle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs148981726 | 2:27,476,699 | A/G | downstream gene variant | — |
| rs2465412836 | 2:27,478,191 | G/A | — | uncertain significance |
| rs779570928 | 2:27,478,193 | G/C | — | uncertain significance |
| rs1676782321 | 2:27,478,202 | C/T | — | uncertain significance |
| rs776225136 | 2:27,478,220 | A/G | — | uncertain significance |
| rs138075294 | 2:27,478,227 | G/A | — | uncertain significance |
| rs140122355 | 2:27,479,255 | G/T | — | benign |
| rs374976347 | 2:27,479,280 | T/A | — | uncertain significance |
| rs948551513 | 2:27,479,314 | C/T | — | uncertain significance |
| rs1227936370 | 2:27,479,326 | G/A | — | uncertain significance |
| rs778531415 | 2:27,479,335 | G/A | — | uncertain significance |
| rs538009364 | 2:27,479,339 | C/T | — | likely benign |
| rs956968053 | 2:27,479,355 | C/T | — | uncertain significance |
| rs73924411 | 2:27,479,503 | C/T | intron variant | — |
| rs762380280 | 2:27,480,036 | G/A | — | uncertain significance |
| rs756037276 | 2:27,480,105 | C/T | — | uncertain significance |
| rs375191770 | 2:27,480,167 | C/T | — | uncertain significance |
| rs148758588 | 2:27,480,186 | G/T | — | uncertain significance |
| rs555500903 | 2:27,480,191 | G/T | — | uncertain significance |
| rs1572471322 | 2:27,480,778 | G/A | — | likely benign |
| rs368210448 | 2:27,480,851 | C/T | — | uncertain significance |
| rs201138508 | 2:27,480,895 | G/A | — | likely benign |
| rs146590310 | 2:27,480,908 | G/A | — | uncertain significance |
| rs78757682 | 2:27,480,935 | G/T | — | likely benign |
| rs756363639 | 2:27,481,107 | T/A | — | uncertain significance |
| rs41288821 | 2:27,481,661 | G/A | — | benign |
| rs200038718 | 2:27,481,680 | C/T | — | likely benign |
| rs368825097 | 2:27,481,710 | G/A | — | uncertain significance |
| rs529940740 | 2:27,481,713 | G/A | — | uncertain significance |
| rs762290567 | 2:27,481,808 | G/A | — | likely benign |
| rs11126936 | 2:27,483,101 | G/A | — | — |
| rs766989486 | 2:27,485,714 | G/C | — | uncertain significance |
| rs186711987 | 2:27,487,135 | T/C | regulatory region variant | — |
| rs114561490 | 2:27,487,702 | T/C | regulatory region variant | — |
| rs6547521 | 2:27,488,432 | G/A | — | — |
| rs72817537 | 2:27,497,549 | G/A | upstream gene variant | — |
| rs4665961 | 2:27,500,381 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.