Variant: rs1553961516 

    present in Gene: ZEB2
    present in Chromosome: 2
    Position on Chromosome: 144398578
    Alleles of this Variant: G/T

rs1553961516 in ZEB2 gene and Dysmorphic features PMID 21343952 2011 Clinical utility gene card for: Mowat-Wilson syndrome.

PMID 19842203 2009 Comprehensive ZEB2 gene analysis for Mowat-Wilson syndrome in a North American cohort: a suggested approach to molecular diagnostics.

PMID 26809768 2016 A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson Syndrome.

PMID 16053902 2005 Clinical and mutational spectrum of Mowat-Wilson syndrome.

PMID 17958891 2007 Mowat-Wilson syndrome.

PMID 26721324 2016 Early Infantile Epileptic Encephalopathy with a de novo variant in ZEB2 identified by exome sequencing.

PMID 27831545 2017 Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients.

PMID 19764019 2009 Mandibuloacral dysplasia type A in childhood.

rs1553961516 in ZEB2 gene and Muscle hypotonia PMID 17958891 2007 Mowat-Wilson syndrome.

PMID 16053902 2005 Clinical and mutational spectrum of Mowat-Wilson syndrome.

PMID 19764019 2009 Mandibuloacral dysplasia type A in childhood.

PMID 26721324 2016 Early Infantile Epileptic Encephalopathy with a de novo variant in ZEB2 identified by exome sequencing.

PMID 27831545 2017 Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients.

PMID 19842203 2009 Comprehensive ZEB2 gene analysis for Mowat-Wilson syndrome in a North American cohort: a suggested approach to molecular diagnostics.

PMID 21343952 2011 Clinical utility gene card for: Mowat-Wilson syndrome.

PMID 26809768 2016 A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson Syndrome.