NOD2 NM_001370466.1(NOD2):c.2093C>G (p.Ala698Gly)

CI-VAR-00053479Explore in graph →p.Ala698GlyNM_001370466.1:c.2093C>GClinVar 319461 rs5743278

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.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
319461	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Blau syndrome; Inflammatory bowel disease 1; Autoinflammatory syndrome; Yao syndrome; Regional enteritis; Lung cancer; Cervical cancer; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma	germline	10	Jun 01, 2026	clinvar