Variant: rs372754256 

    present in Gene: FLG;FLG-AS1
    present in Chromosome: 1
    Position on Chromosome: 152307855
    Alleles of this Variant: G/C

rs372754256 in FLG;FLG-AS1 gene and Dysmorphic features PMID 24267886 2013 Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.

PMID 22542183 2012 De novo gene disruptions in children on the autistic spectrum.

PMID 20790920 1966 Clinical features of autosomal dominant and sex-linked ichthyosis in an English population.

PMID 21173567 2011 Filaggrin gene defects and the risk of developing allergic disorders.

PMID 16444271 2006 Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.

PMID 17417636 2007 Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.

rs372754256 in FLG;FLG-AS1 gene and Movement Disorders PMID 22542183 2012 De novo gene disruptions in children on the autistic spectrum.

PMID 21173567 2011 Filaggrin gene defects and the risk of developing allergic disorders.

PMID 24267886 2013 Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.

PMID 20790920 1966 Clinical features of autosomal dominant and sex-linked ichthyosis in an English population.

PMID 16444271 2006 Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.

PMID 17417636 2007 Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.

rs372754256 in FLG;FLG-AS1 gene and Muscle hypotonia PMID 21173567 2011 Filaggrin gene defects and the risk of developing allergic disorders.

PMID 17417636 2007 Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.

PMID 22542183 2012 De novo gene disruptions in children on the autistic spectrum.

PMID 24267886 2013 Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.

PMID 20790920 1966 Clinical features of autosomal dominant and sex-linked ichthyosis in an English population.

PMID 16444271 2006 Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.