Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918792
rs121918792
SCN1A ; SCN1A-AS1 ; LOC102724058
0.010 GeneticVariation BEFREE A different substitution (G1674R) at the same amino acid position, as well as two other SCN1A mutations found in this study, had previously been reported in Dravet syndrome. 26311622

2015