Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908919
rs121908919
Entrez Id: 6335;101929680
Gene Symbol: SCN9A;SCN1A-AS1
SCN9A;SCN1A-AS1
CUI: C2751778
Disease:
Generalized Epilepsy With Febrile Seizures Plus, 7
0.800 GeneticVariation UNIPROT A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome. 19763161 2009
dbSNP: rs121908919
rs121908919
Entrez Id: 6335;101929680
Gene Symbol: SCN9A;SCN1A-AS1
SCN9A;SCN1A-AS1
CUI: C2751778
Disease:
Generalized Epilepsy With Febrile Seizures Plus, 7
C 0.800 CausalMutation CLINVAR