Variant: rs398122416 

    present in Gene: MAGEL2
    present in Chromosome: 15
    Position on Chromosome: 23645941
    Alleles of this Variant: G/-

rs398122416 in MAGEL2 gene and Prader-Willi-like syndrome PMID 24076603 2013 Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism.