Variant: rs121918628 

    present in Gene: SCN1A-AS1;LOC102724058;SCN1A
    present in Chromosome: 2
    Position on Chromosome: 165998049
    Alleles of this Variant: G/T

rs121918628 in SCN1A-AS1;LOC102724058;SCN1A gene and Migraine, Familial Hemiplegic, 3 PMID 17397047 2007 The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.

PMID 16054936 2005 Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.

PMID 18021921 2007 Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3.

PMID 19332696 2009 Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.