List of variants in gene HCN1 reported as benign by Ambry Genetics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_021072.4(HCN1):c.1710C>T (p.Asn570=)	rs141455774	0.00038
NM_021072.4(HCN1):c.159C>G (p.His53Gln)	rs10066808	0.00019
NM_021072.4(HCN1):c.261C>G (p.Pro87=)	rs199612501	0.00003
NM_021072.4(HCN1):c.1146G>A (p.Gly382=)
NM_021072.4(HCN1):c.192TGGCGGCGG[1] (p.Gly72_Gly74del)	rs56064803

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