Variant · Snv
DNAJB2 NM_006736.6(DNAJB2):c.230-2A>G
CI-VAR-00037437Explore in graph →NM_006736.6:c.230-2A>GClinVar 234675 rs369661561
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 |
|---|---|---|---|---|---|---|---|---|
| 234675 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Neuronopathy, distal hereditary motor, autosomal recessive 5; Charcot-Marie-Tooth disease type 2; Inborn genetic diseases; Thyroid cancer, nonmedullary, 1; Familial cancer of breast; Cervical cancer | germline | 10 | Jan 26, 2026 | clinvar |