List of variants in gene HCN1 reported as likely pathogenic for not provided

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_021072.4(HCN1):c.1148C>T (p.Ala383Val)	rs2112040707
NM_021072.4(HCN1):c.1191C>G (p.Ile397Met)	rs2112040618
NM_021072.4(HCN1):c.1201G>A (p.Asp401Asn)	rs587777491
NM_021072.4(HCN1):c.779C>T (p.Thr260Ile)
NM_021072.4(HCN1):c.858C>A (p.His286Gln)	rs765728211
NM_021072.4(HCN1):c.913A>T (p.Met305Leu)	rs1057521989

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