PEX10 NM_002617.4(PEX10):c.600+1G>A

CI-VAR-00005617Explore in graph →NM_002617.4:c.600+1G>AClinVar 6770 rs267608183

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
6770	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Peroxisome biogenesis disorder 6A (Zellweger); Peroxisome biogenesis disorder, complementation group 7; Peroxisome biogenesis disorder 6B; Peroxisome biogenesis disorder; Zellweger spectrum disorders; Lymphoma; PEX10-related disorder	germline	10	Sep 29, 2025	clinvar