Variant · Snv
CDH23 NM_022124.6(CDH23):c.8980-14C>A
CI-VAR-00008702Explore in graph →NM_022124.6:c.8980-14C>AClinVar 46062 rs45522532
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 |
|---|---|---|---|---|---|---|---|---|
| 46062 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Usher syndrome type 1D; Autosomal recessive nonsyndromic hearing loss 12; Gastric cancer; Uterine corpus endometrial carcinoma; Ovarian serous cystadenocarcinoma; Thymoma; Acute myeloid leukemia; Lung cancer | germline | 8 | May 01, 2026 | clinvar |