Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918628
rs121918628
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. 19332696

2009
dbSNP: rs121918632
rs121918632
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. 19332696

2009
dbSNP: rs121918633
rs121918633
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. 19332696

2009
dbSNP: rs121918628
rs121918628
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT 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. 17397047

2007
dbSNP: rs121918628
rs121918628
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. 18021921

2007
dbSNP: rs121918632
rs121918632
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. 18021921

2007
dbSNP: rs121918632
rs121918632
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT 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. 17397047

2007
dbSNP: rs121918633
rs121918633
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. 18021921

2007
dbSNP: rs121918633
rs121918633
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT 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. 17397047

2007
dbSNP: rs121918628
rs121918628
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. 16054936

2005
dbSNP: rs121918632
rs121918632
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. 16054936

2005
dbSNP: rs121918633
rs121918633
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. 16054936

2005
dbSNP: rs121918628
rs121918628
SCN1A ; SCN1A-AS1 ; LOC102724058
T 0.800 CausalMutation CLINVAR

dbSNP: rs121918632
rs121918632
SCN1A ; SCN1A-AS1 ; LOC102724058
G 0.800 CausalMutation CLINVAR

dbSNP: rs121918633
rs121918633
SCN1A ; SCN1A-AS1 ; LOC102724058
G 0.800 CausalMutation CLINVAR

dbSNP: rs121918799
rs121918799
SCN1A ; SCN1A-AS1 ; LOC102724058
0.700 GeneticVariation UNIPROT Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. 19332696

2009
dbSNP: rs121918799
rs121918799
SCN1A ; SCN1A-AS1 ; LOC102724058
0.700 GeneticVariation UNIPROT Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. 18021921

2007
dbSNP: rs121918799
rs121918799
SCN1A ; SCN1A-AS1 ; LOC102724058
0.700 GeneticVariation UNIPROT 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. 17397047

2007
dbSNP: rs121918799
rs121918799
SCN1A ; SCN1A-AS1 ; LOC102724058
0.700 GeneticVariation UNIPROT Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. 16054936

2005
dbSNP: rs121917964
rs121917964
SCN1A ; SCN1A-AS1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs121917976
rs121917976
SCN1A ; SCN1A-AS1 ; LOC102724058
T 0.700 CausalMutation CLINVAR

dbSNP: rs121917984
rs121917984
SCN1A ; SCN1A-AS1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121918624
rs121918624
SCN1A ; SCN1A-AS1
A 0.700 CausalMutation CLINVAR

dbSNP: rs139300715
rs139300715
SCN1A ; SCN1A-AS1 ; LOC102724058
T 0.700 CausalMutation CLINVAR

dbSNP: rs398123585
rs398123585
SCN1A ; SCN1A-AS1
A 0.700 CausalMutation CLINVAR