Variant: rs1555923822 

    present in Gene: TCF20
    present in Chromosome: 22
    Position on Chromosome: 42210236
    Alleles of this Variant: -/T

rs1555923822 in TCF20 gene and Dysmorphic features PMID 25228304 2014 De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.

PMID 25533962 2015 Large-scale discovery of novel genetic causes of developmental disorders.

PMID 27436265 2016 De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.

PMID 18351660 2008 Discovery of transcription factors and other candidate regulators of neural crest development.

PMID 27479843 2016 Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.

PMID 17151600 2007 Genome-wide atlas of gene expression in the adult mouse brain.

PMID 28135719 2017 Prevalence and architecture of de novo mutations in developmental disorders.

rs1555923822 in TCF20 gene and Movement Disorders PMID 17151600 2007 Genome-wide atlas of gene expression in the adult mouse brain.

PMID 18351660 2008 Discovery of transcription factors and other candidate regulators of neural crest development.

PMID 27479843 2016 Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.

PMID 25533962 2015 Large-scale discovery of novel genetic causes of developmental disorders.

PMID 27436265 2016 De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.

PMID 28135719 2017 Prevalence and architecture of de novo mutations in developmental disorders.

PMID 25228304 2014 De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.

rs1555923822 in TCF20 gene and Muscle hypotonia PMID 27479843 2016 Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.

PMID 28135719 2017 Prevalence and architecture of de novo mutations in developmental disorders.

PMID 18351660 2008 Discovery of transcription factors and other candidate regulators of neural crest development.

PMID 25533962 2015 Large-scale discovery of novel genetic causes of developmental disorders.

PMID 27436265 2016 De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.

PMID 25228304 2014 De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.

PMID 17151600 2007 Genome-wide atlas of gene expression in the adult mouse brain.