Variant: rs121918799 

    present in Gene: SCN1A-AS1;SCN1A;LOC102724058
    present in Chromosome: 2
    Position on Chromosome: 166015636
    Alleles of this Variant: G/C

rs121918799 in SCN1A-AS1;SCN1A;LOC102724058 gene and Epilepsy, Rolandic PMID 29358611 2018 Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.

rs121918799 in SCN1A-AS1;SCN1A;LOC102724058 gene and Migraine, Familial Hemiplegic, 3 PMID 16054936 2005 Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.

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