rs1057518759, CDKL5

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Epileptic encephalopathy
CUI: C0543888
Disease: Epileptic encephalopathy
0.700 GeneticVariation CLINVAR
Developmental delay (disorder)
CUI: C0424605
Disease: Developmental delay (disorder)
0.700 GeneticVariation CLINVAR