Variant: rs767961672 

    present in Gene: FOXG1
    present in Chromosome: 14
    Position on Chromosome: 28767822
    Alleles of this Variant: G/A;T

rs767961672 in FOXG1 gene and FOXG1 syndrome PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs767961672 in FOXG1 gene and Generalized hypotonia PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs767961672 in FOXG1 gene and Microcephaly (physical finding) PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.

rs767961672 in FOXG1 gene and Moderate intellectual disability PMID 26938784 2016 A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.