Variant: rs1334099693 

    present in Gene: SOX4
    present in Chromosome: 6
    Position on Chromosome: 21594732
    Alleles of this Variant: C/A;T

rs1334099693 in SOX4 gene and Clinodactyly of the 5th finger PMID 30661772 2019 De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

rs1334099693 in SOX4 gene and Constipation PMID 30661772 2019 De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

rs1334099693 in SOX4 gene and Deglutition Disorders PMID 30661772 2019 De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

rs1334099693 in SOX4 gene and Exaggerated cupid's bow PMID 30661772 2019 De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

rs1334099693 in SOX4 gene and Feeding difficulties in infancy PMID 30661772 2019 De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

rs1334099693 in SOX4 gene and Intrauterine retardation PMID 30661772 2019 De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

rs1334099693 in SOX4 gene and Macrostomia PMID 30661772 2019 De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

rs1334099693 in SOX4 gene and Posteriorly rotated ear PMID 30661772 2019 De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

rs1334099693 in SOX4 gene and Progressive microcephaly PMID 30661772 2019 De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

rs1334099693 in SOX4 gene and Seizures PMID 30661772 2019 De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.

rs1334099693 in SOX4 gene and Ventricular Septal Defects PMID 30661772 2019 De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.