RS1057519548 HCN1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Epileptic encephalopathy
Developmental and epileptic encephalopathy
24
Inborn genetic diseases
Epileptic encephalopathy
Developmental and epileptic encephalopathy
24
Inborn genetic diseases
Other Variants in HCN1