SCNN1A NM_001038.6(SCNN1A):c.1853G>T (p.Cys618Phe)

CI-VAR-00031653Explore in graph →p.Cys618PheNM_001038.6:c.1853G>TClinVar 194190 rs3741913

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
194190	Benign	criteria provided, multiple submitters, no conflicts	2	Bronchiectasis with or without elevated sweat chloride 2; Pseudohypoaldosteronism, type IB1, autosomal recessive; Clear cell carcinoma of kidney	germline	9	Jan 27, 2026	clinvar