rs10462087, HCN1

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Childhood Absence Epilepsy
CUI: C4281785
Disease: Childhood 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
Absence Epilepsy
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