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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HCN2
(S126L)
Single nucleotide variant
(missense variant)
Febrile seizures, familial, 2
GPathogenic
HCN2
(V246M)
Single nucleotide variant
(missense variant)
Febrile seizures, familial, 2
Grisk factor
HCN2
Single nucleotide variant
(missense variant)
Febrile seizures, familial, 2
Grisk factor
HCN2
(S632W)
Single nucleotide variant
(missense variant)
Febrile seizures, familial, 2
Grisk factor
HCN2
Microsatellite
(inframe_deletion)
not specified
+1 more
GBenign
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