SCN9A NM_001365536.1(SCN9A):c.1314+1G>A

CI-VAR-00334013Explore in graph →NM_001365536.1:c.1314+1G>AClinVar 2943921 rs1295192882

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
2943921	Likely pathogenic	criteria provided, single submitter	1	Neuropathy, hereditary sensory and autonomic, type 2A; Generalized epilepsy with febrile seizures plus, type 7; Uterine corpus endometrial carcinoma	germline	2	Feb 23, 2023	clinvar