Variant · Snv
ZFYVE26 NM_015346.4(ZFYVE26):c.6987-3C>T
CI-VAR-00044420Explore in graph →NM_015346.4:c.6987-3C>TClinVar 241058 rs76728509
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 241058 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Hereditary spastic paraplegia 15; Spastic paraplegia; Hereditary spastic paraplegia; Acute myeloid leukemia; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Lung cancer; Clear cell carcinoma of kidney; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Cervical cancer | germline | 11 | Jan 31, 2026 | clinvar |