CHD8 Chromosome 14

Chromodomain helicase DNA binding protein 8
270 variants 270 Health Risk

Upload your DNA to see your personal genotypes for variants in CHD8.

What This Gene Does
This gene encodes a member of the chromodomain-helicase-DNA binding protein family, which is characterized by a SNF2-like domain and two chromatin organization modifier domains. The encoded protein also contains brahma and kismet domains, which are common to the subfamily of chromodomain-helicase-DNA binding proteins to which this protein belongs. This gene has been shown to function in several processes that include transcriptional regulation, epigenetic remodeling, promotion of cell proliferation, and regulation of RNA synthesis. Allelic variants of this gene are associated with autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2016]
Gene Info
Gene Group
"SNF2 related family|Small nucleolar RNA protein coding host genes"
Locus Type
gene with protein product
Location
14q11.2
Ensembl
ENSG00000100888
Associated Conditions (22)
Intellectual developmental disorder with autism and macrocephaly
Inborn genetic diseases
Autism spectrum disorder
CHD8-related disorder
Congenital ptosis
Overgrowth
Fatigable weakness
Increased muscle fatiguability
Macrocephaly
Complex neurodevelopmental disorder
See cases
Intellectual disability
Developmental disorder
Marfanoid habitus and intellectual disability
Neurodevelopmental disorder
CHD8-associated Neurodevelopmental syndrome
Rare genetic intellectual disability
Familial prostate cancer
Uterine corpus endometrial carcinoma
Glioma susceptibility 1
+2 more conditions
Key Variants
All Variants (270)
RSID Category Clinical Significance Conditions
RS374435577 Health Risk Conflicting classifications of pathogenicity Intellectual developmental disorder with autism and macrocephaly, Inborn genetic diseases, Intellectual developmental disorder with autism and macrocephaly
RS376260777 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CHD8-related disorder, Inborn genetic diseases
RS376527943 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS377109513 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS377359922 Health Risk Conflicting classifications of pathogenicity
RS377595194 Health Risk Conflicting classifications of pathogenicity Intellectual developmental disorder with autism and macrocephaly, Inborn genetic diseases, Intellectual developmental disorder with autism and macrocephaly
RS530700201 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Complex neurodevelopmental disorder, Inborn genetic diseases
RS545239905 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS553367989 Health Risk Conflicting classifications of pathogenicity Intellectual developmental disorder with autism and macrocephaly, Inborn genetic diseases, CHD8-related disorder
RS565918098 Health Risk Conflicting classifications of pathogenicity Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS573063062 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS61752839 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS745375504 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CHD8-related disorder, Inborn genetic diseases
RS745726816 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS745891727 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, See cases, Inborn genetic diseases
RS746163664 Health Risk Conflicting classifications of pathogenicity CHD8-related disorder, Inborn genetic diseases, Intellectual developmental disorder with autism and macrocephaly
RS747289672 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Intellectual developmental disorder with autism and macrocephaly, Inborn genetic diseases
RS748109741 Health Risk Conflicting classifications of pathogenicity
RS749752534 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS75084078 Health Risk Conflicting classifications of pathogenicity
RS751773278 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS751815253 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS752375264 Health Risk Conflicting classifications of pathogenicity
RS752493285 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS753061978 Health Risk Conflicting classifications of pathogenicity
RS753886912 Health Risk Conflicting classifications of pathogenicity Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS754553508 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS755292321 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS755646683 Health Risk Conflicting classifications of pathogenicity Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS759628921 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS760362633 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS761808046 Health Risk Conflicting classifications of pathogenicity
RS762427755 Health Risk Conflicting classifications of pathogenicity CHD8-related disorder, Intellectual developmental disorder with autism and macrocephaly, CHD8-related disorder
RS763248373 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS763843295 Health Risk Conflicting classifications of pathogenicity
RS763909898 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS765571443 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS766317271 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS766456579 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS766944646 Health Risk Conflicting classifications of pathogenicity See cases, See cases
RS767023297 Health Risk Conflicting classifications of pathogenicity Intellectual developmental disorder with autism and macrocephaly, Inborn genetic diseases, Intellectual developmental disorder with autism and macrocephaly
RS769253036 Health Risk Conflicting classifications of pathogenicity Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS770184277 Health Risk Conflicting classifications of pathogenicity Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS771079174 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Intellectual disability, Inborn genetic diseases
RS771590165 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS771925976 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS772660830 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Intellectual developmental disorder with autism and macrocephaly, Inborn genetic diseases
RS774630592 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS775667283 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS777851125 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
Sign Up to Analyze Your DNA Log In