Gene: SCN1A ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs794726713
rs794726713
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT

dbSNP: rs1057517958
rs1057517958
SCN1A ; SCN1A-AS1 ; LOC102724058
0.700 GeneticVariation UNIPROT

dbSNP: rs1057521079
rs1057521079
SCN1A ; SCN1A-AS1 ; LOC102724058
0.700 GeneticVariation UNIPROT

dbSNP: rs1057521080
rs1057521080
SCN1A ; SCN1A-AS1
0.700 GeneticVariation UNIPROT

dbSNP: rs1131691465
rs1131691465
SCN1A ; SCN1A-AS1
0.700 GeneticVariation UNIPROT

dbSNP: rs1131691675
rs1131691675
SCN1A ; SCN1A-AS1 ; LOC102724058
0.700 GeneticVariation UNIPROT

dbSNP: rs1131691774
rs1131691774
SCN1A ; SCN1A-AS1 ; LOC102724058
0.700 GeneticVariation UNIPROT

dbSNP: rs1131691775
rs1131691775
SCN1A ; SCN1A-AS1 ; LOC102724058
0.700 GeneticVariation UNIPROT

dbSNP: rs566081370
rs566081370
SCN1A ; SCN1A-AS1 ; LOC102724058
0.700 GeneticVariation UNIPROT

dbSNP: rs745378416
rs745378416
SCN1A ; SCN1A-AS1
0.700 GeneticVariation UNIPROT

dbSNP: rs758871507
rs758871507
SCN1A ; SCN1A-AS1
0.700 GeneticVariation UNIPROT

dbSNP: rs796052964
rs796052964
SCN1A ; SCN1A-AS1
0.700 GeneticVariation UNIPROT

dbSNP: rs796052973
rs796052973
SCN1A ; SCN1A-AS1
0.700 GeneticVariation UNIPROT

dbSNP: rs796053089
rs796053089
SCN1A ; SCN1A-AS1
0.700 GeneticVariation UNIPROT

dbSNP: rs796053095
rs796053095
SCN1A ; SCN1A-AS1
0.700 GeneticVariation UNIPROT

dbSNP: rs121917915
rs121917915
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures. 12566275

2003
dbSNP: rs121917915
rs121917915
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A. 14672992

2003
dbSNP: rs121917915
rs121917915
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy. 12754708

2003
dbSNP: rs121917915
rs121917915
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy. 12821740

2003
dbSNP: rs121917918
rs121917918
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A. 14672992

2003
dbSNP: rs121917918
rs121917918
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy. 12754708

2003
dbSNP: rs121917918
rs121917918
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy. 12821740

2003
dbSNP: rs121917918
rs121917918
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures. 12566275

2003
dbSNP: rs121917921
rs121917921
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy. 12754708

2003
dbSNP: rs121917921
rs121917921
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures. 12566275

2003