Gene entry
CHD8
chromodomain helicase DNA binding protein 8
- Chromosome
- 14
- Cytoband
- 14q11.2
- Variants (rsID)
- 12
CHD8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q11.2). Its official name is “chromodomain helicase DNA binding protein 8”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs10467770Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs61752837Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs111250264Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder
- rs201604061Conflicting interpretationssingle nucleotide variantAutism, susceptibility to, 18
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.