Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397514600
rs397514600
NOL3
0.700 GeneticVariation UNIPROT Screening of mutations in NOL3 in a myoclonic syndromes series. 25138476

2014
dbSNP: rs397514600
rs397514600
NOL3
0.700 GeneticVariation UNIPROT Familial cortical myoclonus with a mutation in NOL3. 22926851

2012