Variant: rs886039763 

    present in Gene: RPL36A-HNRNPH2;HNRNPH2
    present in Chromosome: X
    Position on Chromosome: 101412604
    Alleles of this Variant: C/T

rs886039763 in RPL36A-HNRNPH2;HNRNPH2 gene and Dysmorphic features PMID 27545675 2016 Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in Females.

PMID 25348405 2015 UniProt: a hub for protein information.

PMID 25356899 2014 De novo mutations in moderate or severe intellectual disability.

rs886039763 in RPL36A-HNRNPH2;HNRNPH2 gene and MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE PMID 27545675 2016 Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in Females.

rs886039763 in RPL36A-HNRNPH2;HNRNPH2 gene and Muscle hypotonia PMID 25348405 2015 UniProt: a hub for protein information.

PMID 25356899 2014 De novo mutations in moderate or severe intellectual disability.

PMID 27545675 2016 Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in Females.