ORC1 NM_004153.4(ORC1):c.2159G>A (p.Arg720Gln)

CI-VAR-00006741Explore in graph →p.Arg720GlnNM_004153.4:c.2159G>AClinVar 30233 rs387906828

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
30233	Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Meier-Gorlin syndrome 1; Fetal anomalies with a likely genetic cause	germline	5	Mar 25, 2026	clinvar