List of variants in gene HCN4 reported as benign by PreventionGenetics, part of Exact Sciences

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_005477.3(HCN4):c.3600A>G (p.Pro1200=)	rs529004	0.88237
NM_005477.3(HCN4):c.1979-41A>G	rs481579	0.80894
NM_005477.3(HCN4):c.1558C>T (p.Leu520=)	rs12909882	0.07848
NM_005477.3(HCN4):c.2556G>A (p.Pro852=)	rs117819825	0.04888
NM_005477.3(HCN4):c.107G>A (p.Gly36Glu)	rs143090627	0.04452
NM_005477.3(HCN4):c.3337A>G (p.Met1113Val)	rs142735148	0.00983
NM_005477.3(HCN4):c.36C>G (p.Leu12=)	rs201193660	0.00635
NM_005477.3(HCN4):c.2601C>A (p.Ala867=)	rs143188160	0.00352
NM_005477.3(HCN4):c.2657C>T (p.Ala886Val)	rs200575377	0.00352
NM_005477.3(HCN4):c.1518C>T (p.Tyr506=)	rs139590882	0.00163
NM_005477.3(HCN4):c.3117G>A (p.Pro1039=)	rs749785521	0.00011
NM_005477.3(HCN4):c.1243G>A (p.Val415Met)	rs201978086	0.00007
NM_005477.3(HCN4):c.2700C>A (p.Ala900=)	rs377656260

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