Gene entry
CEP41
centrosomal protein 41
- Chromosome
- 7
- Cytoband
- 7q32.2
- Variants (rsID)
- 18
CEP41 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q32.2). Its official name is “centrosomal protein 41”. The reference table lists 18 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs113941736Benignsingle nucleotide variantJoubert syndrome 15
- rs11765434Benignsingle nucleotide variantJoubert syndrome 15
- rs17133175Benignsingle nucleotide variantJoubert syndrome 15
- rs2287371Benignsingle nucleotide variantJoubert syndrome 15
- rs7793239Benignsingle nucleotide variantJoubert syndrome 15
- rs143303575Conflicting interpretationssingle nucleotide variantJoubert syndrome 15|Familial Autism Spectrum Disorder
- rs147444165Conflicting interpretationssingle nucleotide variantJoubert syndrome 15
- rs782460743Conflicting interpretationssingle nucleotide variantJoubert syndrome|Joubert syndrome 15
- rs145808545Uncertain significancesingle nucleotide variantJoubert syndrome 15
- rs201834429Uncertain significancesingle nucleotide variantJoubert syndrome 15
- rs368178632Uncertain significancesingle nucleotide variantJoubert syndrome 9/15, digenic|Joubert syndrome 15|Familial Autism Spectrum Disorder
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.