CHRNB1 NM_000747.3(CHRNB1):c.1045-6C>G

CI-VAR-00031888Explore in graph →NM_000747.3:c.1045-6C>GClinVar 199037 rs79209506

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
199037	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Congenital myasthenic syndrome 2A; Congenital myasthenic syndrome 4C; Thymoma; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus	germline	11	Feb 01, 2026	clinvar