CLCN2 NM_004366.6(CLCN2):c.898+1G>A

CI-VAR-00197795Explore in graph →NM_004366.6:c.898+1G>AClinVar 1194517 rs141074059

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
1194517	Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Familial hyperaldosteronism type II; Epilepsy, idiopathic generalized, susceptibility to, 11; Leukoencephalopathy with mild cerebellar ataxia and white matter edema; Uterine corpus endometrial carcinoma	germline	4	Mar 04, 2024	clinvar