List of variants in gene HCN1 reported as uncertain significance by New York Genome Center

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_021072.4(HCN1):c.1777C>G (p.Arg593Gly)	rs989268235	0.00003
NM_021072.4(HCN1):c.1377+19834C>T	rs761223261
NM_021072.4(HCN1):c.2165C>T (p.Pro722Leu)	rs2111839334
NM_021072.4(HCN1):c.849+66420G>T	rs986310668

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