SLC22A24
solute carrier family 22 member 24
Summary
SLC22A24 belongs to a large family of transmembrane proteins that function as uniporters, symporters, and antiporters to transport organic ions across cell membranes (Jacobsson et al., 2007 [PubMed 17714910]).[supplied by OMIM, Mar 2008]
Known Variants66 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs139977495 | 11:62,847,420 | G/C | — | uncertain significance |
| rs1288177039 | 11:62,848,407 | T/C | — | uncertain significance |
| rs370756811 | 11:62,848,518 | G/A | — | likely benign |
| rs1287521623 | 11:62,848,563 | C/G | — | uncertain significance |
| rs142507239 | 11:62,848,585 | C/A | — | uncertain significance |
| rs1381436255 | 11:62,849,057 | T/C | — | uncertain significance |
| rs1170367441 | 11:62,849,060 | T/C | — | uncertain significance |
| rs2539699496 | 11:62,850,739 | G/C | — | uncertain significance |
| rs1047710524 | 11:62,850,783 | C/T | — | uncertain significance |
| rs777717825 | 11:62,850,787 | G/A | — | uncertain significance |
| rs1252328396 | 11:62,850,793 | T/C | — | uncertain significance |
| rs1280192332 | 11:62,850,844 | C/T | — | uncertain significance |
| rs1310046577 | 11:62,850,846 | C/T | — | uncertain significance |
| rs1357391704 | 11:62,850,922 | T/C | — | uncertain significance |
| rs118186763 | 11:62,852,423 | T/A | intron variant | — |
| rs111275386 | 11:62,852,999 | G/A | intron variant | — |
| rs182462158 | 11:62,858,802 | A/G | intron variant | — |
| rs150262653 | 11:62,860,465 | A/G | intron variant | — |
| rs1317639393 | 11:62,863,498 | T/G | — | uncertain significance |
| rs754245809 | 11:62,863,503 | G/T | — | uncertain significance |
| rs528111522 | 11:62,863,509 | G/A | — | uncertain significance |
| rs370535827 | 11:62,863,526 | G/A | — | uncertain significance |
| rs376030248 | 11:62,863,575 | C/G | — | uncertain significance |
| rs112545435 | 11:62,865,521 | C/T | — | — |
| rs113444667 | 11:62,870,065 | G/A | intron variant | — |
| rs374446472 | 11:62,871,698 | T/A | — | uncertain significance |
| rs976025979 | 11:62,871,730 | G/C | — | uncertain significance |
| rs112621169 | 11:62,872,235 | G/A | intron variant | — |
| rs141232858 | 11:62,874,534 | A/C | intron variant | — |
| rs183044805 | 11:62,875,348 | C/A | — | — |
| rs374672720 | 11:62,878,603 | T/G | — | — |
| rs142056054 | 11:62,880,411 | C/G | — | — |
| rs113939203 | 11:62,882,727 | T/A | downstream gene variant | — |
| rs147641133 | 11:62,882,800 | G/T | downstream gene variant | — |
| rs2087231097 | 11:62,886,402 | A/G | — | uncertain significance |
| rs1468108609 | 11:62,886,475 | G/A | — | uncertain significance |
| rs1046685801 | 11:62,886,483 | C/T | — | uncertain significance |
| rs2539047858 | 11:62,886,495 | G/T | — | uncertain significance |
| rs1005664752 | 11:62,886,531 | C/T | — | likely benign |
| rs764546704 | 11:62,886,547 | C/T | — | uncertain significance |
| rs2539047938 | 11:62,886,549 | A/G | — | uncertain significance |
| rs747797825 | 11:62,886,673 | A/C | — | uncertain significance |
| rs1280005607 | 11:62,886,699 | C/G | — | uncertain significance |
| rs116063135 | 11:62,886,706 | C/A | — | uncertain significance |
| rs557316228 | 11:62,886,737 | C/T | — | uncertain significance |
| rs906604172 | 11:62,886,778 | C/T | — | uncertain significance |
| rs118072533 | 11:62,899,582 | G/T | intron variant | — |
| rs185441216 | 11:62,902,157 | T/C | — | uncertain significance |
| rs752239055 | 11:62,902,179 | C/A | — | uncertain significance |
| rs116782537 | 11:62,904,545 | G/T | — | — |
| rs11231379 | 11:62,904,935 | C/G | upstream gene variant | — |
| rs113172275 | 11:62,905,115 | T/C | upstream gene variant | — |
| rs761345188 | 11:62,910,897 | C/T | — | uncertain significance |
| rs1388097576 | 11:62,910,905 | C/T | — | uncertain significance |
| rs561816044 | 11:62,910,914 | G/A | — | uncertain significance |
| rs765183890 | 11:62,910,941 | G/T | — | uncertain significance |
| rs778023107 | 11:62,910,961 | C/A | — | uncertain significance |
| rs770233577 | 11:62,910,975 | G/T | — | uncertain significance |
| rs556942414 | 11:62,910,984 | G/T | — | uncertain significance |
| rs370028693 | 11:62,911,059 | C/T | — | uncertain significance |
| rs769230112 | 11:62,911,061 | G/T | — | uncertain significance |
| rs2539067841 | 11:62,911,114 | A/C | — | uncertain significance |
| rs772474998 | 11:62,911,121 | G/T | — | uncertain significance |
| rs779534196 | 11:62,911,168 | G/T | — | uncertain significance |
| rs4366490 | 11:62,912,854 | T/A | — | — |
| rs79586456 | 11:62,913,582 | G/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.