Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918632
rs121918632
SCN1A ; SCN1A-AS1 ; LOC102724058
0.010 GeneticVariation BEFREE Results In both pedigrees, we identified SCN1A mutation p.F1499L, which has been previously associated with familial hemiplegic migraine type 3 and elicited repetitive daily blindness. 29145747

2018