"Blueprint Genetics"[submitter] AND "HCN4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 636407	NM_005477.3(HCN4):c.2605G>A (p.Ala869Thr)	HCN4 (A869T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 636394	NM_005477.3(HCN4):c.2482C>T (p.Arg828Trp)	HCN4 (R828W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 222649	NM_005477.3(HCN4):c.2261A>G (p.His754Arg)	HCN4 (H754R)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 222648	NM_005477.3(HCN4):c.2197G>A (p.Val733Ile)	HCN4 (V733I)	Single nucleotide variant (missense variant)	Brugada syndrome 8 +5 more	GUncertain significance
Select item 222647	NM_005477.3(HCN4):c.1732C>T (p.Arg578Trp)	HCN4 (R578W)	Single nucleotide variant (missense variant)	Brugada syndrome 8 +1 more	GUncertain significance
Select item 222646	NM_005477.3(HCN4):c.559G>A (p.Ala187Thr)	HCN4 (A187T)	Single nucleotide variant (missense variant)	Brugada syndrome 8 +1 more	GUncertain significance
Select item 180370	NM_005477.3(HCN4):c.458A>G (p.Glu153Gly)	HCN4 (E153G)	Single nucleotide variant (missense variant)	not provided +7 more	GConflicting classifications of pathogenicity

ClinVar