List of variants in gene KCNH2 reported as uncertain significance by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.442C>T (p.Arg148Trp)	rs139544114	0.00062
NM_000238.4(KCNH2):c.526C>T (p.Arg176Trp)	rs36210422	0.00061
NM_000238.4(KCNH2):c.2738C>T (p.Ala913Val)	rs77331749	0.00056
NM_000238.4(KCNH2):c.865G>A (p.Glu289Lys)	rs199472880	0.00009
NM_000238.4(KCNH2):c.422C>T (p.Pro141Leu)	rs199472864	0.00007
NM_000238.4(KCNH2):c.2717C>T (p.Ser906Leu)	rs199473435	0.00004
NM_000238.4(KCNH2):c.3097C>T (p.Arg1033Trp)	rs199473021	0.00004
NM_000238.4(KCNH2):c.1703G>C (p.Trp568Ser)	rs1554425880
NM_000238.4(KCNH2):c.206T>A (p.Leu69Gln)	rs199473665
NM_000238.4(KCNH2):c.2398+3A>G	rs1554425151
NM_000238.4(KCNH2):c.3125T>C (p.Leu1042Pro)	rs886039064
NM_000238.4(KCNH2):c.3453_3454del (p.His1151fs)	rs1554423346

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