Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906420
rs387906420
TRNF
C 0.700 CausalMutation CLINVAR Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) gene. 20142618

2010