HNF1B NM_000458.4(HNF1B):c.592A>C (p.Ser198Arg)

CI-VAR-00101019Explore in graph →p.Ser198ArgNM_000458.4:c.592A>CClinVar 546210 rs1321074352

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
546210	Uncertain significance/Uncertain risk allele	criteria provided, multiple submitters, no conflicts	2	Nonpapillary renal cell carcinoma; Renal cysts and diabetes syndrome; Type 2 diabetes mellitus; Maturity-onset diabetes of the young	germline	4	Oct 23, 2025	clinvar