Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398123593
rs398123593
SCN1A ; SCN1A-AS1 ; LOC102724058
0.010 GeneticVariation BEFREE Postnatal day 15-21 heterozygous SCN1A-R1407X knock-in mice, expressing a human Dravet syndrome mutation, were used to investigate a possible cardiac phenotype. 24155976

2013