DSG2 NM_001943.5(DSG2):c.2744G>C (p.Arg915Thr)

CI-VAR-00054610Explore in graph →p.Arg915ThrNM_001943.5:c.2744G>CClinVar 326486 rs375358300

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
326486	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Arrhythmogenic right ventricular dysplasia 10; Cardiomyopathy; Cardiovascular phenotype; Dilated cardiomyopathy 1BB; Arrhythmogenic right ventricular cardiomyopathy; Familial cancer of breast	germline	10	Jan 18, 2026	clinvar