Gene entry
TELO2
telomere maintenance 2
- Chromosome
- 16
- Cytoband
- 16p13.3
- Variants (rsID)
- 14
TELO2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.3). Its official name is “telomere maintenance 2”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs202020308Conflicting interpretationssingle nucleotide variantTELO2-related intellectual disability-neurodevelopmental disorder
- rs371675497Conflicting interpretationssingle nucleotide variantTELO2-related intellectual disability-neurodevelopmental disorder
- rs878853271Conflicting interpretationssingle nucleotide variantTELO2-related intellectual disability-neurodevelopmental disorder
- rs369656775Pathogenicsingle nucleotide variantTELO2-related intellectual disability-neurodevelopmental disorder
- rs754162070Pathogenicsingle nucleotide variantTELO2-related intellectual disability-neurodevelopmental disorder
- rs2667661Not classifiedmissense_variant
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.
