Variant: rs397514600 

    present in Gene: NOL3
    present in Chromosome: 16
    Position on Chromosome: 67174230
    Alleles of this Variant: G/C

rs397514600 in NOL3 gene and MYOCLONUS, FAMILIAL CORTICAL PMID 25138476 2014 Screening of mutations in NOL3 in a myoclonic syndromes series.

PMID 22926851 2012 Familial cortical myoclonus with a mutation in NOL3.