Variant: rs786200952 

    present in Gene: KAT6A
    present in Chromosome: 8
    Position on Chromosome: 41934340
    Alleles of this Variant: -/T

rs786200952 in KAT6A gene and Bulbous nose PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

rs786200952 in KAT6A gene and Clinodactyly of the 5th finger PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

rs786200952 in KAT6A gene and Craniosynostosis PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

rs786200952 in KAT6A gene and Delayed speech and language development PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

rs786200952 in KAT6A gene and Feeding difficulties PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

rs786200952 in KAT6A gene and Hemangioma PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

rs786200952 in KAT6A gene and Microcephaly (physical finding) PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

rs786200952 in KAT6A gene and Muscle hypotonia PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

rs786200952 in KAT6A gene and Narrow forehead PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

rs786200952 in KAT6A gene and Poor school performance PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

rs786200952 in KAT6A gene and Wide spaced nipples PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

rs786200952 in KAT6A gene and obsolete Abnormal heart morphology PMID 25728777 2015 Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.