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 A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. 16122630

2005
dbSNP: rs121917918
rs121917918
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. 16122630

2005
dbSNP: rs121917921
rs121917921
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. 16122630

2005
dbSNP: rs121917922
rs121917922
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. 16122630

2005
dbSNP: rs121917923
rs121917923
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. 16122630

2005
dbSNP: rs121917927
rs121917927
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. 16122630

2005
dbSNP: rs121917929
rs121917929
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. 16122630

2005
dbSNP: rs121917935
rs121917935
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. 16122630

2005
dbSNP: rs121917937
rs121917937
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. 16122630

2005
dbSNP: rs121917938
rs121917938
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. 16122630

2005