Gene entry
ORC1
origin recognition complex subunit 1
- Chromosome
- 1
- Cytoband
- 1p32.3
- Variants (rsID)
- 11
ORC1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p32.3). Its official name is “origin recognition complex subunit 1”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs3087473Benignsingle nucleotide variantMeier-Gorlin syndrome 1
- rs3087476Benignsingle nucleotide variantMeier-Gorlin syndrome 1
- rs34521609Benignsingle nucleotide variantMeier-Gorlin syndrome 1
- rs61753390Benignsingle nucleotide variantMeier-Gorlin syndrome 1
- rs143141689Pathogenicsingle nucleotide variantMeier-Gorlin syndrome 1|Meier-Gorlin syndrome
- rs201253919Uncertain significancesingle nucleotide variantMeier-Gorlin syndrome 1
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.