List of variants in gene HCN4 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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_005477.3(HCN4):c.3209G>A (p.Gly1070Asp)	rs772839442	0.00004
NM_005477.3(HCN4):c.497C>T (p.Pro166Leu)	rs771442346	0.00004
NM_005477.3(HCN4):c.3293C>T (p.Ala1098Val)	rs1064797200	0.00003
NM_005477.3(HCN4):c.2309C>A (p.Thr770Lys)	rs763021264
NM_005477.3(HCN4):c.286_297del (p.Phe96_Ser99del)

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