Variant: rs1566446604 

    present in Gene: CHD8
    present in Chromosome: 14
    Position on Chromosome: 21431511
    Alleles of this Variant: GAGAGCTTGGCAGTCCA/-

rs1566446604 in CHD8 gene and AUTISM, SUSCEPTIBILITY TO, 18 PMID 26789910 2016 A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.

PMID 24998929 2014 Disruptive CHD8 mutations define a subtype of autism early in development.

PMID 23160955 2012 Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

PMID 22495309 2012 Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.

rs1566446604 in CHD8 gene and Autistic Disorder PMID 22495309 2012 Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.

PMID 23160955 2012 Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

PMID 26789910 2016 A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.

PMID 24998929 2014 Disruptive CHD8 mutations define a subtype of autism early in development.

rs1566446604 in CHD8 gene and Eczema PMID 22495309 2012 Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.

PMID 26789910 2016 A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.

PMID 23160955 2012 Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

PMID 24998929 2014 Disruptive CHD8 mutations define a subtype of autism early in development.

rs1566446604 in CHD8 gene and Overgrowth PMID 23160955 2012 Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

PMID 22495309 2012 Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.

PMID 26789910 2016 A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.

PMID 24998929 2014 Disruptive CHD8 mutations define a subtype of autism early in development.

rs1566446604 in CHD8 gene and Poor school performance PMID 23160955 2012 Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

PMID 26789910 2016 A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.

PMID 22495309 2012 Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.

PMID 24998929 2014 Disruptive CHD8 mutations define a subtype of autism early in development.

rs1566446604 in CHD8 gene and Seizures PMID 24998929 2014 Disruptive CHD8 mutations define a subtype of autism early in development.

PMID 22495309 2012 Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.

PMID 26789910 2016 A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.

PMID 23160955 2012 Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.