KRT17 NM_000422.3(KRT17):c.834+5G>A

CI-VAR-00132268Explore in graph →NM_000422.3:c.834+5G>AClinVar 773316 rs190234778

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
773316	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Pachyonychia congenita 2; Steatocystoma multiplex; KRT17-related disorder; Cervical cancer; Clear cell carcinoma of kidney; Gastric cancer; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Malignant tumor of esophagus; Lung cancer; Familial cancer of breast	germline	6	Jan 31, 2026	clinvar