Variant · Snv
NDRG1 NM_006096.4(NDRG1):c.892-5C>T
CI-VAR-00051935Explore in graph →NM_006096.4:c.892-5C>TClinVar 362033 rs2233346
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 |
|---|---|---|---|---|---|---|---|---|
| 362033 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Charcot-Marie-Tooth disease type 4; Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease type 4D; Lung cancer; Cervical cancer; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Gastric cancer; Ovarian serous cystadenocarcinoma; Cholangiocarcinoma; Nonpapillary renal cell carcinoma; Uterine carcinosarcoma; Acute myeloid leukemia | germline | 9 | Feb 01, 2026 | clinvar |