rs1162306056, KCNQ3

N. diseases: 5
Disease: EPILEPSY, BENIGN NEONATAL, 2 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
EPILEPSY, BENIGN NEONATAL, 2
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
0.010 GeneticVariation BEFREE The mutation in KCNQ3, c.989G>A, was novel and occurred in an infant with BFNS. 25052858 2014