NRXN1 NM_001330078.2(NRXN1):c.569A>G (p.Asn190Ser)

CI-VAR-00025849Explore in graph →p.Asn190SerNM_001330078.2:c.569A>GClinVar 167390 rs200792504

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
167390	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Pitt-Hopkins-like syndrome 2; Chromosome 2p16.3 deletion syndrome; Intellectual disability; Inborn genetic diseases; Adrenocortical carcinoma, hereditary	germline	13	Jan 18, 2026	clinvar