List of variants in gene HCN4 reported as uncertain significance for not specified

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_005477.3(HCN4):c.1331A>T (p.Asp444Val)	rs1444329166	0.00001
NM_005477.3(HCN4):c.3388G>A (p.Gly1130Arg)	rs1326171404	0.00001
NM_005477.3(HCN4):c.1963G>A (p.Gly655Ser)
NM_005477.3(HCN4):c.2797G>T (p.Ala933Ser)	rs762464413
NM_005477.3(HCN4):c.2804C>T (p.Ser935Phe)	rs775803239
NM_005477.3(HCN4):c.3100C>T (p.Pro1034Ser)	rs1158677290
NM_005477.3(HCN4):c.3497_3500del (p.Ser1166fs)	rs774674047
NM_005477.3(HCN4):c.514C>T (p.Pro172Ser)
NM_005477.3(HCN4):c.76A>G (p.Met26Val)

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