Gene entry
CR2
complement C3d receptor 2
- Chromosome
- 1
- Cytoband
- 1q32.2
- Variants (rsID)
- 14
CR2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q32.2). Its official name is “complement C3d receptor 2”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs17615Benignsingle nucleotide variantImmunodeficiency, common variable, 7
- rs34349246Benignsingle nucleotide variantImmunodeficiency, common variable, 7
- rs143614333Conflicting interpretationssingle nucleotide variantImmunodeficiency, common variable, 7
- rs151093663Conflicting interpretationssingle nucleotide variantImmunodeficiency, common variable, 7
- rs142206860Uncertain significancesingle nucleotide variantImmunodeficiency, common variable, 7
- rs145499318Uncertain significancesingle nucleotide variantImmunodeficiency, common variable, 7
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.