Variant: rs199476396 

    present in Gene: AGRN
    present in Chromosome: 1
    Position on Chromosome: 1050575
    Alleles of this Variant: G/C

rs199476396 in AGRN gene and Myasthenic Syndromes, Congenital PMID 19631309 2009 Identification of an agrin mutation that causes congenital myasthenia and affects synapse function.