ABCC8 NM_000352.6(ABCC8):c.2117-3C>T

CI-VAR-00025041Explore in graph →NM_000352.6:c.2117-3C>TClinVar 157688 rs1799854

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
157688	Benign	criteria provided, multiple submitters, no conflicts	2	Permanent neonatal diabetes mellitus; Diabetes mellitus, transient neonatal, 2; Hyperinsulinemic hypoglycemia, familial, 1; Hereditary hyperinsulinism; Leucine-induced hypoglycemia; Diabetes mellitus, permanent neonatal 3; Type 2 diabetes mellitus; Familial cancer of breast	germline/somatic	15	Feb 04, 2026	clinvar