VPS50
VPS50 subunit of EARP/GARPII complex
Summary
Enables SNARE binding activity. Acts upstream of or within endocytic recycling. Located in recycling endosome. Part of EARP complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs747891799 | 7:92,869,233 | C/T | — | uncertain significance |
| rs537957263 | 7:92,869,234 | G/A | — | uncertain significance |
| rs556549825 | 7:92,875,576 | T/G | — | — |
| rs2535684481 | 7:92,881,975 | A/G | — | uncertain significance |
| rs1224080069 | 7:92,885,845 | A/G | — | uncertain significance |
| rs751830889 | 7:92,887,506 | C/A | — | uncertain significance |
| rs374485392 | 7:92,887,538 | C/T | — | uncertain significance |
| rs1285062805 | 7:92,888,869 | A/G | — | uncertain significance |
| rs372089506 | 7:92,888,934 | A/C | — | uncertain significance |
| rs768885678 | 7:92,902,023 | A/G | — | uncertain significance |
| rs1371713602 | 7:92,905,562 | G/A | — | uncertain significance |
| rs768286481 | 7:92,921,019 | T/G | — | uncertain significance |
| rs199896068 | 7:92,921,139 | C/T | — | uncertain significance |
| rs1246040612 | 7:92,923,883 | G/A | — | uncertain significance |
| rs200434482 | 7:92,926,077 | C/G | — | likely benign |
| rs374290264 | 7:92,926,102 | A/G | — | uncertain significance |
| rs2546590713 | 7:92,926,489 | G/C | — | uncertain significance |
| rs1157958323 | 7:92,926,556 | G/T | — | uncertain significance |
| rs755983691 | 7:92,935,228 | T/C | — | uncertain significance |
| rs2546600294 | 7:92,935,309 | C/T | — | uncertain significance |
| rs1562879672 | 7:92,938,176 | A/G | — | uncertain significance |
| rs1265974629 | 7:92,938,197 | C/T | — | uncertain significance |
| rs1262620713 | 7:92,938,211 | C/T | — | likely pathogenic |
| rs2546603981 | 7:92,938,229 | C/T | — | likely pathogenic |
| rs779281256 | 7:92,940,483 | C/A | — | uncertain significance |
| rs2546606508 | 7:92,940,572 | A/G | — | uncertain significance |
| rs2188404 | 7:92,943,760 | T/C | intron variant | — |
| rs758851279 | 7:92,952,983 | T/A | — | uncertain significance |
| rs770778444 | 7:92,953,034 | G/A | — | uncertain significance |
| rs745695719 | 7:92,963,428 | G/T | — | pathogenic |
| rs771305740 | 7:92,963,481 | A/G | — | uncertain significance |
| rs761124862 | 7:92,970,778 | G/A | — | uncertain significance |
| rs376216197 | 7:92,970,845 | C/T | — | uncertain significance |
| rs373044128 | 7:92,983,035 | A/C | — | uncertain significance |
| rs61741161 | 7:92,985,211 | A/G | — | benign |
| rs2546648415 | 7:92,985,273 | A/G | — | uncertain significance |
| rs1395453962 | 7:92,985,297 | A/G | — | uncertain significance |
| rs3764799 | 7:92,985,305 | C/G | — | benign |
| rs752338408 | 7:92,985,307 | T/C | — | uncertain significance |
| rs1798696932 | 7:92,985,310 | C/T | — | uncertain significance |
| rs148888740 | 7:92,985,347 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.