WWOX NM_016373.4(WWOX):c.606-1G>A

CI-VAR-00027094Explore in graph →NM_016373.4:c.606-1G>AClinVar 183303 rs730882215

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
183303	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Abnormal facial shape; Brain atrophy; Global developmental delay; Developmental and epileptic encephalopathy, 28; Developmental and epileptic encephalopathy, 1; Autosomal recessive spinocerebellar ataxia 12; WWOX-related disorder; Esophageal squamous cell carcinoma	germline	10	Oct 07, 2025	clinvar