Gene entry
CDON
cell adhesion associated, oncogene regulated
- Chromosome
- 11
- Cytoband
- 11q24.2
- Variants (rsID)
- 42
CDON is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q24.2). Its official name is “cell adhesion associated, oncogene regulated”. The reference table lists 42 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs113921147Benignsingle nucleotide variantHoloprosencephaly 11
- rs115533243Benignsingle nucleotide variantHoloprosencephaly 11
- rs12274923Benignsingle nucleotide variantHoloprosencephaly 11
- rs35131477Benignsingle nucleotide variantHoloprosencephaly 11
- rs35665264Benignsingle nucleotide variantHoloprosencephaly 11
- rs35884952Benignsingle nucleotide variantHoloprosencephaly 11
- rs3740904Benignsingle nucleotide variantHoloprosencephaly 11
- rs3740912Benignsingle nucleotide variantHoloprosencephaly 11
- rs4937076Benignsingle nucleotide variantHoloprosencephaly sequence
- rs73628538Benignsingle nucleotide variantHoloprosencephaly 11
- rs387906995Likely pathogenicsingle nucleotide variantHoloprosencephaly 11
Other listed variants
- rs538107
- rs560640
- rs564016
- rs599702
- rs625280
- rs670263
- rs718443
- rs2043438
- rs4288765
- rs4420284
- rs4540843
- rs11220295
- rs11220301
- rs11220316
- rs11220321
- rs11220329
- rs61917839
- rs73021218
- rs73629836
- rs76526512
- rs77915153
- rs79548354
- rs79989050
- rs113615738
- rs140364205
- rs145157571
- rs182489399
- rs186192833
- rs189366163
- rs200008378
- rs568524587
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.