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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HCN1
(M487T)
Single nucleotide variant
(missense variant)
Generalized epilepsy with febrile seizures plus, type 10
GUncertain significance
HCN1
(H310Y)
Single nucleotide variant
(missense variant)
Generalized epilepsy with febrile seizures plus, type 10
+1 more
GUncertain significance