WT1 NM_024426.6(WT1):c.1074A>G (p.Gln358=)

CI-VAR-00047392Explore in graph →p.Gln358=NM_024426.6:c.1074A>GClinVar 261708 rs2234590

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
261708	Benign	criteria provided, multiple submitters, no conflicts	2	Nephrotic syndrome, type 4; Wilms tumor 1; Meacham syndrome; Frasier syndrome; Drash syndrome; 11p partial monosomy syndrome; Kidney disorder; Inborn genetic diseases	germline	18	Feb 03, 2026	clinvar