List of variants in gene combination HCN4, LOC105370890 reported as uncertain significance for Brugada syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005477.3(HCN4):c.1178G>A (p.Arg393His)	rs786205804
NM_005477.3(HCN4):c.1190A>C (p.Tyr397Ser)	rs2043016094
NM_005477.3(HCN4):c.1209+2_1209+3insGTGA	rs786205418
NM_005477.3(HCN4):c.1209+3A>G
NM_005477.3(HCN4):c.1209+4A>G	rs2043015976

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