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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HCN4
(S1005F)
Single nucleotide variant
(missense variant)
Brugada syndrome 8
GUncertain significance
HCN4
(P928A)
Single nucleotide variant
(missense variant)
Brugada syndrome 8
GUncertain significance
HCN4
(A23T)
Single nucleotide variant
(missense variant)
Brugada syndrome 8
GUncertain significance
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