Variant: rs1554404013 

    present in Gene: RELN
    present in Chromosome: 7
    Position on Chromosome: 103697970
    Alleles of this Variant: G/T

rs1554404013 in RELN gene and Dysmorphic features PMID 10973257 2000 Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.

PMID 16958033 2007 The role of RELN in lissencephaly and neuropsychiatric disease.

PMID 11748497 2001 Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations.

PMID 17431900 2007 Identification of a novel recessive RELN mutation using a homozygous balanced reciprocal translocation.

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

PMID 25621899 2015 Whole-genome sequencing of quartet families with autism spectrum disorder.

PMID 26046367 2015 Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.

PMID 17955477 2008 The association analysis of RELN and GRM8 genes with autistic spectrum disorder in Chinese Han population.

PMID 25648840 2015 RELN rare variants in myoclonus-dystonia.