Disease: Migraine, Familial Hemiplegic, 3 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918628
rs121918628
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.800 GeneticVariation UNIPROT Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. 19332696 2009
dbSNP: rs121918632
rs121918632
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.800 GeneticVariation UNIPROT Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. 19332696 2009
dbSNP: rs121918633
rs121918633
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.800 GeneticVariation UNIPROT Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. 19332696 2009
dbSNP: rs121918628
rs121918628
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		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
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.800 GeneticVariation UNIPROT Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. 18021921 2007
dbSNP: rs121918632
rs121918632
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.800 GeneticVariation UNIPROT Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. 18021921 2007
dbSNP: rs121918632
rs121918632
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		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
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.800 GeneticVariation UNIPROT Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. 18021921 2007
dbSNP: rs121918633
rs121918633
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		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
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.800 GeneticVariation UNIPROT Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. 16054936 2005
dbSNP: rs121918632
rs121918632
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.800 GeneticVariation UNIPROT Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. 16054936 2005
dbSNP: rs121918633
rs121918633
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.800 GeneticVariation UNIPROT Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. 16054936 2005
dbSNP: rs121918628
rs121918628
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		T 0.800 CausalMutation CLINVAR
dbSNP: rs121918632
rs121918632
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		G 0.800 CausalMutation CLINVAR
dbSNP: rs121918633
rs121918633
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		G 0.800 CausalMutation CLINVAR
dbSNP: rs121918799
rs121918799
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.700 GeneticVariation UNIPROT Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. 19332696 2009
dbSNP: rs121918799
rs121918799
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.700 GeneticVariation UNIPROT Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. 18021921 2007
dbSNP: rs121918799
rs121918799
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		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
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		0.700 GeneticVariation UNIPROT Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. 16054936 2005
dbSNP: rs121917964
rs121917964
Entrez Id: 6323;101929680
Gene Symbol: SCN1A;SCN1A-AS1
SCN1A;SCN1A-AS1
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs121917976
rs121917976
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121917984
rs121917984
Entrez Id: 6323;101929680
Gene Symbol: SCN1A;SCN1A-AS1
SCN1A;SCN1A-AS1
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121918624
rs121918624
Entrez Id: 6323;101929680
Gene Symbol: SCN1A;SCN1A-AS1
SCN1A;SCN1A-AS1
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		A 0.700 CausalMutation CLINVAR
dbSNP: rs139300715
rs139300715
Entrez Id: 6323;101929680;102724058
Gene Symbol: SCN1A;SCN1A-AS1;LOC102724058
SCN1A;SCN1A-AS1;LOC102724058
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		T 0.700 CausalMutation CLINVAR
dbSNP: rs398123585
rs398123585
Entrez Id: 6323;101929680
Gene Symbol: SCN1A;SCN1A-AS1
SCN1A;SCN1A-AS1
CUI: C1864987
Disease:
Migraine, Familial Hemiplegic, 3 		A 0.700 CausalMutation CLINVAR