Variant: rs1555313219 

    present in Gene: CHD8;SNORD9
    present in Chromosome: 14
    Position on Chromosome: 21393500
    Alleles of this Variant: C/A;T

rs1555313219 in CHD8;SNORD9 gene and AUTISM, SUSCEPTIBILITY TO, 18 PMID 24998929 2014 Disruptive CHD8 mutations define a subtype of autism early in development.

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

rs1555313219 in CHD8;SNORD9 gene and Poor school performance 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 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.