Variant: rs1568318932 

    present in Gene: NFIX
    present in Chromosome: 19
    Position on Chromosome: 13075673
    Alleles of this Variant: T/C

rs1568318932 in NFIX gene and Malan overgrowth syndrome PMID 25118028 2015 Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature.

PMID 20673863 2010 Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndrome.

rs1568318932 in NFIX gene and Marshall-Smith syndrome PMID 25118028 2015 Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature.

PMID 20673863 2010 Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndrome.