HNF1A NM_000545.8(HNF1A):c.139G>C (p.Gly47Arg)

CI-VAR-00153423Explore in graph →p.Gly47ArgNM_000545.8:c.139G>CClinVar 882461 rs373180062

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
882461	Uncertain significance	reviewed by expert panel	3	Maturity-onset diabetes of the young type 3; Monogenic diabetes; Maturity-onset diabetes of the young; Hereditary breast ovarian cancer syndrome	germline	8	Feb 06, 2026	clinvar