Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267608665
rs267608665
RS1 ; CDKL5
0.010 GeneticVariation BEFREE A novel p.Arg970X mutation in the last exon of the CDKL5 gene resulting in late-onset seizure disorder. 19428276

2010