SLC44A5
solute carrier family 44 member 5
Summary
Enables choline transmembrane transporter activity. Involved in choline transport. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs755624816 | 1:75,672,314 | A/G | — | uncertain significance |
| rs756119033 | 1:75,672,326 | T/C | — | uncertain significance |
| rs2523399082 | 1:75,672,387 | T/A | — | uncertain significance |
| rs1436683562 | 1:75,679,392 | G/C | — | uncertain significance |
| rs1195158761 | 1:75,679,436 | A/G | — | uncertain significance |
| rs750397625 | 1:75,679,476 | C/T | — | likely benign |
| rs1208652919 | 1:75,679,607 | T/C | — | uncertain significance |
| rs764887023 | 1:75,679,634 | G/C | — | uncertain significance |
| rs2523457042 | 1:75,680,314 | T/C | — | uncertain significance |
| rs2523467640 | 1:75,681,519 | A/G | — | uncertain significance |
| rs532260637 | 1:75,684,293 | C/T | — | uncertain significance |
| rs533864932 | 1:75,684,419 | T/C | — | uncertain significance |
| rs1647027018 | 1:75,684,968 | G/C | — | uncertain significance |
| rs1343393624 | 1:75,685,488 | G/A | — | uncertain significance |
| rs368493474 | 1:75,685,528 | T/A | — | uncertain significance |
| rs200504981 | 1:75,685,545 | T/C | — | uncertain significance |
| rs1181419149 | 1:75,688,130 | A/G | — | uncertain significance |
| rs1447431108 | 1:75,693,467 | C/T | — | uncertain significance |
| rs778747660 | 1:75,693,500 | C/T | — | likely benign |
| rs1411584963 | 1:75,699,712 | A/T | — | uncertain significance |
| rs777965736 | 1:75,704,234 | C/A | — | uncertain significance |
| rs764439209 | 1:75,707,706 | G/A | — | uncertain significance |
| rs368039703 | 1:75,707,709 | G/T | — | uncertain significance |
| rs2523680104 | 1:75,707,736 | T/C | — | uncertain significance |
| rs376030186 | 1:75,716,945 | G/A | — | uncertain significance |
| rs76985288 | 1:75,741,206 | T/C | — | — |
| rs768547762 | 1:75,766,344 | A/G | — | uncertain significance |
| rs1249675 | 1:75,770,625 | C/G | — | — |
| rs1249662 | 1:75,786,415 | A/G | intron variant | — |
| rs757434928 | 1:75,805,295 | G/C | — | uncertain significance |
| rs911788056 | 1:75,862,291 | G/A | — | uncertain significance |
| rs1857353 | 1:75,913,826 | C/T | intron variant | — |
| rs116362708 | 1:75,930,314 | G/A | intron variant | — |
| rs75726608 | 1:75,999,964 | A/C | downstream gene variant | — |
| rs76934732 | 1:76,013,268 | G/A | intron variant | — |
| rs211694 | 1:76,069,504 | C/T | — | — |
| rs392691 | 1:76,097,044 | C/A | — | — |
| rs211718 | 1:76,106,675 | T/C | downstream gene variant | — |
| rs12760091 | 1:76,111,673 | C/A | — | — |
| rs180867386 | 1:76,111,674 | A/G | upstream gene variant | — |
| rs12729167 | 1:76,111,678 | A/C | upstream gene variant | — |
| rs6672180 | 1:76,123,973 | C/G | intergenic variant | — |
| rs12125269 | 1:76,125,211 | C/A | intergenic variant | — |
| rs12126155 | 1:76,131,555 | C/T | — | — |
| rs7549167 | 1:76,134,258 | T/C | intergenic variant | — |
| rs7552404 | 1:76,135,946 | A/T | — | — |
| rs6593585 | 1:76,140,273 | G/A | intergenic variant | — |
| rs7513363 | 1:76,143,443 | A/G | regulatory region variant | — |
| rs7515955 | 1:76,143,884 | A/T | regulatory region variant | — |
| rs12087626 | 1:76,148,473 | C/A | — | — |
| rs4949874 | 1:76,161,889 | T/C | intergenic variant | — |
| rs7550949 | 1:76,166,846 | C/G | intergenic variant | — |
| rs150404394 | 1:76,166,982 | C/G | intergenic variant | — |
| rs76963882 | 1:76,167,924 | T/C | intergenic variant | — |
| rs4949876 | 1:76,173,377 | C/G | — | — |
| rs942270 | 1:76,177,332 | G/A | intron variant | — |
| rs1498312 | 1:76,177,849 | C/T | intron variant | — |
| rs11161430 | 1:76,180,878 | C/T | intron variant | — |
| rs11161437 | 1:76,182,512 | T/A | — | — |
| rs12091720 | 1:76,186,949 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.