DNAH1 NM_015512.5(DNAH1):c.7193G>A (p.Arg2398His)

CI-VAR-00073459Explore in graph →p.Arg2398HisNM_015512.5:c.7193G>AClinVar 478488 rs201299120

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
478488	Likely benign	criteria provided, multiple submitters, no conflicts	2	Spermatogenic failure 18; Ciliary dyskinesia, primary, 37; Thyroid cancer, nonmedullary, 1; Adrenocortical carcinoma, hereditary; Acute myeloid leukemia; Familial cancer of breast; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney	germline	6	Feb 02, 2026	clinvar