Gene: SCN1A-AS1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918735
rs121918735
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918736
rs121918736
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918737
rs121918737
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918738
rs121918738
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918739
rs121918739
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918740
rs121918740
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918741
rs121918741
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918742
rs121918742
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918763
rs121918763
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918768
rs121918768
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918770
rs121918770
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918773
rs121918773
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918775
rs121918775
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918785
rs121918785
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918791
rs121918791
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121918793
rs121918793
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT A mutation in GABRB3 associated with Dravet syndrome. 28544625

2017
dbSNP: rs121917915
rs121917915
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. 26993267

2016
dbSNP: rs121917918
rs121917918
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. 26993267

2016
dbSNP: rs121917921
rs121917921
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. 26993267

2016
dbSNP: rs121917922
rs121917922
SCN1A ; SCN1A-AS1 ; LOC102724058
0.800 GeneticVariation UNIPROT Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. 26993267

2016
dbSNP: rs121917923
rs121917923
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. 26993267

2016
dbSNP: rs121917927
rs121917927
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. 26993267

2016
dbSNP: rs121917929
rs121917929
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. 26993267

2016
dbSNP: rs121917935
rs121917935
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. 26993267

2016
dbSNP: rs121917937
rs121917937
SCN1A ; SCN1A-AS1
0.800 GeneticVariation UNIPROT Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. 26993267

2016