Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs118192249
rs118192249
KCNQ3
0.010 GeneticVariation BEFREE Altered KCNQ3 potassium channel function caused by the W309R pore-helix mutation found in human epilepsy. 18425618

2008