rs13181, KLC3;ERCC2

N. diseases: 134
Disease: Early infantile epileptic encephalopathy with suppression bursts ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Early infantile epileptic encephalopathy with suppression bursts
CUI: C0393706
Disease: Early infantile epileptic encephalopathy with suppression bursts
0.010 GeneticVariation BEFREE With respect to ERCC2 rs13181 polymorphism, this polymorphism was not correlated with the response to chemotherapy for OS patients under all three models. 28388903 2017