Variant · Snv
DSP NM_004415.4(DSP):c.273+5G>A
CI-VAR-00025762Explore in graph →NM_004415.4:c.273+5G>AClinVar 163237 rs200473206
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 |
|---|---|---|---|---|---|---|---|---|
| 163237 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Long QT syndrome; Primary dilated cardiomyopathy; Arrhythmogenic right ventricular cardiomyopathy; Arrhythmogenic cardiomyopathy with wooly hair and keratoderma; Arrhythmogenic right ventricular dysplasia 8; Cardiomyopathy; Lethal acantholytic epidermolysis bullosa; Woolly hair-skin fragility syndrome; Cardiovascular phenotype; Cervical cancer; Colon adenocarcinoma; Familial cancer of breast | germline | 19 | Feb 04, 2026 | clinvar |