Variant: rs1553353206 

    present in Gene: MIR4742;WDR26
    present in Chromosome: 1
    Position on Chromosome: 224398525
    Alleles of this Variant: CATTTAACAA/-

rs1553353206 in MIR4742;WDR26 gene and Dysmorphic features PMID 28686853 2017 WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features.

rs1553353206 in MIR4742;WDR26 gene and Multiple congenital anomalies PMID 28686853 2017 WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features.

rs1553353206 in MIR4742;WDR26 gene and Muscle hypotonia PMID 28686853 2017 WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features.