ClinVar Miner

List of variants in gene HCN4 reported as uncertain significance for cardiac conduction defect

Included ClinVar conditions (6):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005477.3(HCN4):c.2275G>A (p.Val759Ile)	rs62641689	0.00258
NM_005477.3(HCN4):c.1928T>G (p.Leu643Arg)	rs1555475541

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