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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HCN4
(L643R)
Single nucleotide variant
(missense variant)
Sudden cardiac death
+1 more
GUncertain significance
HCN4
(R242C)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
HCN4
(P174S)
Single nucleotide variant
(missense variant)
Sick sinus syndrome 2, autosomal dominant
+5 more
GUncertain significance
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