MYO7A NM_000260.4(MYO7A):c.2904G>A (p.Glu968=)

CI-VAR-00037434Explore in graph →p.Glu968=NM_000260.4:c.2904G>AClinVar 228280 rs111033233

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
228280	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Rare genetic deafness; Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1; Autosomal dominant nonsyndromic hearing loss 11; Thyroid cancer, nonmedullary, 1; Usher syndrome type 1B; MYO7A-related disorder	germline	7	Aug 11, 2025	clinvar