VPS9D1
VPS9 domain containing 1
Summary
Enables identical protein binding activity. Predicted to be involved in proton motive force-driven ATP synthesis. Predicted to be active in cytosol and endocytic vesicle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61747704 | 16:89,774,288 | C/T | — | likely benign |
| rs1398337122 | 16:89,774,860 | C/A | — | uncertain significance |
| rs372082040 | 16:89,774,863 | C/T | — | uncertain significance |
| rs377107520 | 16:89,774,875 | C/T | — | uncertain significance |
| rs777363379 | 16:89,774,890 | C/T | — | uncertain significance |
| rs763052865 | 16:89,775,286 | G/A | — | uncertain significance |
| rs771231445 | 16:89,775,293 | C/T | — | uncertain significance |
| rs975544237 | 16:89,775,319 | G/A | — | uncertain significance |
| rs767333609 | 16:89,775,662 | A/G | — | uncertain significance |
| rs201610914 | 16:89,775,700 | G/T | — | uncertain significance |
| rs759181367 | 16:89,775,701 | C/T | — | uncertain significance |
| rs765146515 | 16:89,775,722 | C/T | — | uncertain significance |
| rs748518295 | 16:89,775,773 | C/T | — | uncertain significance |
| rs768244692 | 16:89,775,826 | C/T | — | uncertain significance |
| rs1000392219 | 16:89,776,227 | G/A | — | uncertain significance |
| rs372981873 | 16:89,776,257 | T/C | — | uncertain significance |
| rs370686335 | 16:89,776,272 | T/G | — | uncertain significance |
| rs374855421 | 16:89,777,039 | G/C | — | uncertain significance |
| rs535269991 | 16:89,777,056 | A/C | missense variant | — |
| rs200129122 | 16:89,777,108 | C/A | — | uncertain significance |
| rs762484469 | 16:89,777,216 | G/A | — | uncertain significance |
| rs2060899762 | 16:89,777,269 | G/A | — | uncertain significance |
| rs1390434948 | 16:89,777,314 | C/T | — | uncertain significance |
| rs527419696 | 16:89,777,345 | C/A | — | uncertain significance |
| rs2060902736 | 16:89,777,366 | A/G | — | uncertain significance |
| rs781492709 | 16:89,777,386 | C/T | — | likely benign |
| rs200050626 | 16:89,777,417 | G/T | — | uncertain significance |
| rs201649648 | 16:89,777,798 | G/C | — | uncertain significance |
| rs201251363 | 16:89,778,290 | A/G | — | benign |
| rs1044172676 | 16:89,778,365 | G/C | — | uncertain significance |
| rs2060955986 | 16:89,778,887 | G/C | — | uncertain significance |
| rs139626173 | 16:89,778,919 | T/C | — | benign |
| rs139714289 | 16:89,781,167 | G/A | intron variant | — |
| rs200980425 | 16:89,782,896 | C/A | — | uncertain significance |
| rs201389166 | 16:89,782,902 | C/A | — | uncertain significance |
| rs759874119 | 16:89,782,963 | C/T | — | uncertain significance |
| rs2061074016 | 16:89,782,969 | T/G | — | uncertain significance |
| rs754677006 | 16:89,782,987 | G/C | — | uncertain significance |
| rs1211462438 | 16:89,782,990 | A/G | — | uncertain significance |
| rs2543865825 | 16:89,783,012 | T/A | — | uncertain significance |
| rs774620484 | 16:89,783,021 | G/C | — | uncertain significance |
| rs755592321 | 16:89,783,168 | C/G | — | uncertain significance |
| rs62068372 | 16:89,785,107 | T/C | upstream gene variant | — |
| rs113661672 | 16:89,785,242 | C/T | upstream gene variant | — |
| rs1452887356 | 16:89,785,456 | C/T | — | uncertain significance |
| rs769945465 | 16:89,785,468 | G/C | — | uncertain significance |
| rs375400111 | 16:89,785,476 | T/C | — | uncertain significance |
| rs34141697 | 16:89,786,121 | A/G | — | — |
| rs111836360 | 16:89,786,649 | A/G | — | — |
| rs2061242996 | 16:89,787,187 | G/C | — | uncertain significance |
| rs760328986 | 16:89,787,235 | G/A | — | uncertain significance |
| rs1011100710 | 16:89,787,247 | C/T | — | uncertain significance |
| rs116853582 | 16:89,788,768 | T/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.