Variant · Deletion
VPS35 NM_018206.6(VPS35):c.915-3del
CI-VAR-00126173Explore in graph →NM_018206.6:c.915-3delClinVar 703789 rs569369937
Curated evidence
Evidence by cancer (0 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 703789 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Parkinson disease 17; Parkinson disease; Familial prostate cancer; Uveal melanoma; Adrenocortical carcinoma, hereditary; Cervical cancer; Familial cancer of breast | germline | 4 | Oct 11, 2023 | clinvar |