Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886040861
rs886040861
0.800 GeneticVariation UNIPROT GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers. 27616483

2016

dbSNP: rs886040861
rs886040861
A 0.800 CausalMutation CLINVAR