SCN9A NM_001365536.1(SCN9A):c.4399-14G>T

CI-VAR-00047062Explore in graph →NM_001365536.1:c.4399-14G>TClinVar 258886 rs112927502

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
258886	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Primary erythromelalgia; Channelopathy-associated congenital insensitivity to pain, autosomal recessive; Paroxysmal extreme pain disorder; Neuropathy, hereditary sensory and autonomic, type 2A; Generalized epilepsy with febrile seizures plus, type 7; Ovarian serous cystadenocarcinoma; Uterine corpus endometrial carcinoma; Sarcoma; Gastric cancer	germline	5	Jan 26, 2026	clinvar