SLC23A2
solute carrier family 23 member 2
Summary
The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two required transporters and the encoded protein accounts for tissue-specific uptake of vitamin C. Previously, this gene had an official symbol of SLC23A1. [provided by RefSeq, Jul 2008]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6037992 | 20:4,837,321 | G/T | — | — |
| rs754878558 | 20:4,837,625 | G/A | — | uncertain significance |
| rs1378819646 | 20:4,837,772 | G/A | — | uncertain significance |
| rs1222566247 | 20:4,837,817 | T/C | — | uncertain significance |
| rs139545711 | 20:4,837,827 | G/A | — | uncertain significance |
| rs72552204 | 20:4,847,551 | A/G | upstream gene variant | — |
| rs2514681666 | 20:4,848,475 | C/A | — | uncertain significance |
| rs762763708 | 20:4,850,569 | G/T | — | likely benign |
| rs34460747 | 20:4,850,644 | G/A | — | benign |
| rs62636560 | 20:4,854,604 | C/A | — | benign |
| rs1110277 | 20:4,854,682 | A/G | synonymous variant | — |
| rs1669378959 | 20:4,855,253 | G/A | — | uncertain significance |
| rs41282100 | 20:4,855,309 | G/A | — | benign |
| rs2298173 | 20:4,864,298 | T/C | — | uncertain significance |
| rs35550945 | 20:4,864,326 | C/T | — | benign |
| rs6116569 | 20:4,864,717 | T/C | downstream gene variant | — |
| rs4987219 | 20:4,864,946 | C/G | downstream gene variant | — |
| rs200887058 | 20:4,865,403 | C/T | — | uncertain significance |
| rs879273161 | 20:4,865,422 | T/A | — | uncertain significance |
| rs763351316 | 20:4,866,476 | T/C | — | uncertain significance |
| rs202059859 | 20:4,880,191 | C/T | — | benign |
| rs760314010 | 20:4,883,135 | T/C | — | uncertain significance |
| rs200765683 | 20:4,883,155 | C/T | — | uncertain significance |
| rs754841827 | 20:4,883,167 | A/G | — | uncertain significance |
| rs756327233 | 20:4,883,200 | G/A | — | uncertain significance |
| rs6133175 | 20:4,891,759 | A/G | intron variant | — |
| rs556171693 | 20:4,893,540 | C/T | — | uncertain significance |
| rs759317661 | 20:4,893,548 | G/A | — | uncertain significance |
| rs116317600 | 20:4,893,559 | C/T | — | benign |
| rs142322986 | 20:4,893,594 | C/T | — | likely benign |
| rs2514731201 | 20:4,893,596 | C/T | — | uncertain significance |
| rs368985081 | 20:4,893,606 | C/A | — | uncertain significance |
| rs895496870 | 20:4,893,608 | C/A | — | uncertain significance |
| rs1715364 | 20:4,898,896 | T/C | intron variant | — |
| rs6139587 | 20:4,942,474 | A/T | regulatory region variant | — |
| rs13037458 | 20:4,951,215 | A/T | — | — |
| rs2681116 | 20:4,951,331 | T/C | intron variant | — |
| rs6139591 | 20:4,951,359 | G/T | — | — |
| rs6053005 | 20:4,957,700 | T/C | intron variant | — |
| rs1519861 | 20:4,974,601 | T/A | intron variant | — |
| rs12479919 | 20:4,980,740 | C/T | intron variant | — |
| rs113708270 | 20:4,982,118 | T/C | — | — |
| rs1279683 | 20:4,983,092 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.