Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518801
rs1057518801
SCN3A
0.710 GeneticVariation BEFREE All patients presented with treatment-resistant epilepsy in the first year of life, severe to profound intellectual disability, and in 2 cases (both with the variant p.Ile875Thr), diffuse polymicrogyria. 29466837

2018
dbSNP: rs1057518801
rs1057518801
SCN3A
G 0.710 GeneticVariation CLINVAR