VPS8
VPS8 subunit of CORVET complex
Summary
Predicted to enable zinc ion binding activity. Involved in endosomal vesicle fusion. Located in early endosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants88 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs372735954 | 3:184,542,478 | G/A | — | uncertain significance |
| rs199778508 | 3:184,543,959 | C/G | — | uncertain significance |
| rs2529668730 | 3:184,543,990 | C/T | — | uncertain significance |
| rs201726179 | 3:184,550,529 | T/C | — | uncertain significance |
| rs532056032 | 3:184,550,538 | T/C | — | uncertain significance |
| rs190794799 | 3:184,552,427 | T/C | — | likely benign |
| rs759084664 | 3:184,552,454 | A/G | — | uncertain significance |
| rs753838943 | 3:184,552,483 | C/T | — | uncertain significance |
| rs200071170 | 3:184,566,906 | G/A | — | uncertain significance |
| rs375080939 | 3:184,566,940 | A/G | — | uncertain significance |
| rs1359067960 | 3:184,567,731 | T/A | — | uncertain significance |
| rs1048271900 | 3:184,567,766 | A/G | — | uncertain significance |
| rs755685702 | 3:184,567,769 | A/G | — | uncertain significance |
| rs887206033 | 3:184,567,773 | A/G | — | uncertain significance |
| rs756731589 | 3:184,570,291 | A/T | — | uncertain significance |
| rs778587238 | 3:184,570,293 | A/G | — | likely benign |
| rs370026889 | 3:184,570,306 | C/G | — | uncertain significance |
| rs2530021449 | 3:184,571,656 | G/C | — | uncertain significance |
| rs762240538 | 3:184,571,686 | T/G | — | uncertain significance |
| rs1724770507 | 3:184,571,728 | A/G | — | uncertain significance |
| rs781090713 | 3:184,571,736 | C/G | — | uncertain significance |
| rs201816956 | 3:184,571,960 | G/A | — | uncertain significance |
| rs16859356 | 3:184,573,603 | A/G | — | benign |
| rs371946822 | 3:184,580,688 | A/G | — | uncertain significance |
| rs1486447376 | 3:184,580,734 | A/G | — | uncertain significance |
| rs944833344 | 3:184,580,755 | A/G | — | uncertain significance |
| rs2530262132 | 3:184,588,549 | T/C | — | uncertain significance |
| rs61742617 | 3:184,603,910 | G/A | — | likely benign |
| rs58693904 | 3:184,612,321 | C/T | — | — |
| rs770129939 | 3:184,612,526 | G/C | — | uncertain significance |
| rs539429882 | 3:184,612,570 | C/A | — | uncertain significance |
| rs2530635853 | 3:184,612,658 | A/C | — | uncertain significance |
| rs1340344426 | 3:184,616,364 | G/T | — | uncertain significance |
| rs560880756 | 3:184,616,392 | A/G | — | likely benign |
| rs1024044364 | 3:184,618,716 | T/G | — | uncertain significance |
| rs2530731709 | 3:184,618,724 | A/G | — | uncertain significance |
| rs779137834 | 3:184,631,322 | T/C | — | uncertain significance |
| rs368160632 | 3:184,632,782 | G/C | — | uncertain significance |
| rs186015852 | 3:184,637,944 | A/G | — | benign |
| rs371510116 | 3:184,642,687 | T/C | — | uncertain significance |
| rs199918828 | 3:184,642,767 | C/G | — | uncertain significance |
| rs1292775992 | 3:184,644,395 | T/G | — | uncertain significance |
| rs769890987 | 3:184,644,410 | A/G | — | uncertain significance |
| rs768378985 | 3:184,646,282 | A/G | — | uncertain significance |
| rs750233890 | 3:184,646,294 | T/A | — | uncertain significance |
| rs750810830 | 3:184,647,448 | G/A | — | uncertain significance |
| rs74927619 | 3:184,648,315 | G/A | — | benign |
| rs2531176563 | 3:184,648,321 | C/G | — | uncertain significance |
| rs755643746 | 3:184,648,339 | G/A | — | uncertain significance |
| rs200456100 | 3:184,654,052 | C/G | — | likely benign |
| rs1170895084 | 3:184,654,086 | T/A | — | uncertain significance |
| rs750036154 | 3:184,654,130 | A/G | — | likely benign |
| rs776037117 | 3:184,658,015 | A/C | — | uncertain significance |
| rs761098684 | 3:184,658,016 | G/T | — | uncertain significance |
| rs2473882899 | 3:184,675,194 | A/G | — | uncertain significance |
| rs1166156497 | 3:184,675,223 | A/G | — | uncertain significance |
| rs201443606 | 3:184,675,247 | C/G | — | uncertain significance |
| rs566967979 | 3:184,675,256 | G/A | — | uncertain significance |
| rs377479838 | 3:184,675,290 | G/A | — | uncertain significance |
| rs2473948692 | 3:184,682,299 | T/C | — | uncertain significance |
| rs527847853 | 3:184,684,474 | C/T | — | uncertain significance |
| rs556078456 | 3:184,689,503 | A/G | — | uncertain significance |
| rs375048106 | 3:184,689,526 | C/G | — | uncertain significance |
| rs371563514 | 3:184,700,367 | C/T | — | uncertain significance |
| rs201685683 | 3:184,700,368 | G/A | — | likely benign |
| rs373192503 | 3:184,700,374 | G/A | — | likely benign |
| rs1750404420 | 3:184,700,411 | G/C | — | uncertain significance |
| rs2474118401 | 3:184,700,432 | G/A | — | uncertain significance |
| rs1192888533 | 3:184,700,820 | C/G | — | uncertain significance |
| rs2474123938 | 3:184,700,850 | G/A | — | uncertain significance |
| rs752280635 | 3:184,711,781 | A/G | — | uncertain significance |
| rs750617628 | 3:184,711,802 | A/G | — | uncertain significance |
| rs777952587 | 3:184,714,121 | C/T | — | uncertain significance |
| rs200270246 | 3:184,714,255 | C/A | — | uncertain significance |
| rs754996312 | 3:184,714,279 | A/G | — | uncertain significance |
| rs751396490 | 3:184,717,503 | T/C | — | uncertain significance |
| rs779201806 | 3:184,717,559 | G/T | — | uncertain significance |
| rs2474269136 | 3:184,717,584 | A/G | — | uncertain significance |
| rs535628675 | 3:184,717,618 | A/T | — | uncertain significance |
| rs780202717 | 3:184,717,628 | G/C | — | uncertain significance |
| rs182147673 | 3:184,731,875 | C/G | intron variant | — |
| rs748806037 | 3:184,742,172 | A/G | — | uncertain significance |
| rs756407039 | 3:184,766,268 | G/A | — | uncertain significance |
| rs1212104561 | 3:184,766,324 | C/T | — | uncertain significance |
| rs16859527 | 3:184,766,325 | G/A | — | benign |
| rs1222490594 | 3:184,769,705 | G/C | — | likely benign |
| rs1212422181 | 3:184,769,740 | C/T | — | uncertain significance |
| rs370499145 | 3:184,769,803 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.