Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918625
rs121918625
SCN1A ; SCN1A-AS1 ; LOC102724058
0.010 GeneticVariation BEFREE In contrast, two other GEFS+ mutations (A1685V and V1353L) and L986F, an SMEI-associated allele, exhibited complete loss of function. 14672992

2003