Variant: rs1553359384 

    present in Gene: WDR26
    present in Chromosome: 1
    Position on Chromosome: 224419530
    Alleles of this Variant: C/T

rs1553359384 in WDR26 gene and SKRABAN-DEARDORFF SYNDROME PMID 28686853 2017 WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features.