Variant: rs121918632 

    present in Gene: LOC102724058;SCN1A-AS1;SCN1A
    present in Chromosome: 2
    Position on Chromosome: 165996099
    Alleles of this Variant: A/G

rs121918632 in LOC102724058;SCN1A-AS1;SCN1A gene and Migraine, Familial Hemiplegic, 3 PMID 19332696 2009 Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.

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.