rs1553798675, FGF12

N. diseases: 4
Disease: Seizures ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Seizures
CUI: C0036572
Disease: Seizures
0.700 GeneticVariation CLINVAR De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy. 27872899 2016