SETX NM_015046.7(SETX):c.7114G>A (p.Asp2372Asn)

CI-VAR-00047306Explore in graph →p.Asp2372AsnNM_015046.7:c.7114G>AClinVar 260517 rs150673589

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
260517	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Amyotrophic lateral sclerosis type 4; Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2; Hereditary spastic paraplegia; Adrenocortical carcinoma, hereditary; Cervical cancer; Clear cell carcinoma of kidney; Hepatocellular carcinoma; Thyroid cancer, nonmedullary, 1	germline	16	Jan 27, 2026	clinvar