Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777162
rs587777162
T 0.700 CausalMutation CLINVAR Exome sequencing reveals new causal mutations in children with epileptic encephalopathies. 23647072

2013

dbSNP: rs587777162
rs587777162
T 0.700 CausalMutation CLINVAR Diagnostic exome sequencing in persons with severe intellectual disability. 23033978

2012