CLCNKB NM_000085.5(CLCNKB):c.968+1G>A

CI-VAR-00200945Explore in graph →NM_000085.5:c.968+1G>AClinVar 1285112 rs201204502

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
1285112	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Bartter disease type 3; Bartter disease type 4B; Autosomal recessive CLCNKB-related disorders; Nonpapillary renal cell carcinoma; CLCNKB-related disorders	germline	10	Dec 11, 2025	clinvar