Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1567135138
rs1567135138
Entrez Id: 1106
Gene Symbol: CHD2
CHD2
CUI: C3809278
Disease:
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET
T 0.700 CausalMutation CLINVAR