CLN6 NM_017882.3(CLN6):c.486+1G>A

CI-VAR-00102057Explore in graph →NM_017882.3:c.486+1G>AClinVar 555430 rs756522171

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
555430	Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Ceroid lipofuscinosis, neuronal, 6A; Neuronal ceroid lipofuscinosis; Inborn genetic diseases; Ceroid lipofuscinosis, neuronal, 6B (Kufs type); CLN6-related disorder; Gastric cancer	germline	7	Nov 19, 2025	clinvar