rs387907281, ATP1A3

N. diseases: 13
Disease: Epilepsy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.010 GeneticVariation BEFREE Genotype-phenotype correlation analysis showed that patients with epilepsy were more likely to carry E815K mutation. 24842602 2014