Disease: Absence Epilepsy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10462087
rs10462087
Entrez Id: 348980
Gene Symbol: HCN1
HCN1
CUI: C0014553
Disease:
Absence Epilepsy 		0.010 GeneticVariation BEFREE The frequency of the HCN1 rs10462087 CC+CT genotype was lower in patients with childhood absence epilepsy (CAE) than controls (P = .047). 29047147 2018