RELCH
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing
Summary
Involved in intracellular cholesterol transport. Located in recycling endosome and trans-Golgi network. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200950948 | 18:59,854,769 | A/C | — | uncertain significance |
| rs367903884 | 18:59,854,770 | G/A | — | uncertain significance |
| rs181701851 | 18:59,854,807 | T/A | — | uncertain significance |
| rs751585155 | 18:59,854,811 | G/A | — | uncertain significance |
| rs2512011578 | 18:59,854,893 | C/G | — | uncertain significance |
| rs545382325 | 18:59,854,941 | G/A | — | uncertain significance |
| rs1169252134 | 18:59,854,965 | C/T | — | uncertain significance |
| rs752153045 | 18:59,854,985 | G/A | — | uncertain significance |
| rs756998932 | 18:59,855,001 | C/A | — | uncertain significance |
| rs2512016474 | 18:59,855,006 | G/A | — | uncertain significance |
| rs761718974 | 18:59,855,178 | T/C | — | uncertain significance |
| rs758399404 | 18:59,855,207 | G/T | — | uncertain significance |
| rs531699202 | 18:59,868,268 | G/A | — | — |
| rs1027720045 | 18:59,878,389 | G/A | — | uncertain significance |
| rs2512263032 | 18:59,878,418 | T/G | — | uncertain significance |
| rs777161330 | 18:59,888,461 | T/G | — | uncertain significance |
| rs765723144 | 18:59,888,476 | G/A | — | uncertain significance |
| rs112542196 | 18:59,891,394 | C/T | intron variant | — |
| rs369560994 | 18:59,894,566 | T/G | — | likely benign |
| rs144111275 | 18:59,894,596 | T/G | — | uncertain significance |
| rs2512405264 | 18:59,894,598 | G/T | — | uncertain significance |
| rs1297000378 | 18:59,894,607 | A/G | — | uncertain significance |
| rs1013775747 | 18:59,894,643 | G/A | — | uncertain significance |
| rs772707448 | 18:59,894,717 | C/T | — | uncertain significance |
| rs552082774 | 18:59,895,580 | A/G | — | benign |
| rs2512417863 | 18:59,895,591 | C/T | — | uncertain significance |
| rs373258912 | 18:59,895,722 | A/G | — | uncertain significance |
| rs371167597 | 18:59,895,738 | A/G | — | uncertain significance |
| rs202119767 | 18:59,895,744 | C/G | — | uncertain significance |
| rs762314033 | 18:59,898,471 | G/A | — | uncertain significance |
| rs3764493 | 18:59,899,576 | T/C | synonymous variant | — |
| rs147104823 | 18:59,899,595 | G/A | — | uncertain significance |
| rs1280441518 | 18:59,899,649 | G/A | — | uncertain significance |
| rs750257764 | 18:59,912,024 | G/A | — | uncertain significance |
| rs386352321 | 18:59,919,898 | C/A | — | uncertain significance |
| rs1054388160 | 18:59,922,644 | A/C | — | uncertain significance |
| rs1290333051 | 18:59,922,703 | T/C | — | uncertain significance |
| rs186300041 | 18:59,922,931 | A/G | intron variant | — |
| rs1443610981 | 18:59,925,309 | C/A | — | uncertain significance |
| rs191406265 | 18:59,925,858 | A/C | — | uncertain significance |
| rs2512734203 | 18:59,925,889 | A/G | — | uncertain significance |
| rs777741251 | 18:59,925,893 | T/C | — | uncertain significance |
| rs142362396 | 18:59,928,768 | C/A | — | uncertain significance |
| rs546632543 | 18:59,928,773 | A/C | — | uncertain significance |
| rs761215171 | 18:59,931,269 | A/G | — | uncertain significance |
| rs2043416166 | 18:59,931,272 | A/G | — | uncertain significance |
| rs759276755 | 18:59,931,281 | C/T | — | uncertain significance |
| rs568940190 | 18:59,932,015 | G/C | — | uncertain significance |
| rs567532043 | 18:59,936,677 | T/G | — | likely benign |
| rs577862335 | 18:59,938,227 | A/T | — | — |
| rs528270513 | 18:59,939,987 | C/T | — | — |
| rs759343103 | 18:59,941,246 | G/A | — | uncertain significance |
| rs143408856 | 18:59,947,597 | C/T | — | uncertain significance |
| rs186712510 | 18:59,949,312 | T/A | regulatory region variant | — |
| rs781468305 | 18:59,949,550 | A/C | — | benign |
| rs561355384 | 18:59,949,653 | G/A | — | uncertain significance |
| rs145936814 | 18:59,954,677 | C/G | — | uncertain significance |
| rs201823885 | 18:59,958,824 | G/A | — | uncertain significance |
| rs370738160 | 18:59,958,830 | G/A | — | uncertain significance |
| rs2045142191 | 18:59,958,847 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.