MYH6 NM_002471.4(MYH6):c.5475G>A (p.Glu1825=)

CI-VAR-00008555Explore in graph →p.Glu1825=NM_002471.4:c.5475G>AClinVar 44537 rs79143968

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
44537	Benign	criteria provided, multiple submitters, no conflicts	2	Hypertrophic cardiomyopathy 14; Cardiovascular phenotype; Cardiomyopathy; Atrial septal defect 3; Dilated cardiomyopathy 1EE; Hypertrophic cardiomyopathy 1; Sick sinus syndrome 3, susceptibility to; Gastric cancer	germline	11	Feb 01, 2026	clinvar