Variants in gene KCNH2 with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.2738C>T (p.Ala913Val)	rs77331749	0.00056
NM_000238.4(KCNH2):c.2371C>T (p.Arg791Trp)	rs138498207	0.00026
NM_000238.4(KCNH2):c.2717C>T (p.Ser906Leu)	rs199473435	0.00004
NM_000238.4(KCNH2):c.2843G>A (p.Arg948His)	rs199473011	0.00003
NM_000238.4(KCNH2):c.2255G>A (p.Arg752Gln)	rs121912512	0.00001
NM_000238.4(KCNH2):c.1675C>T (p.Leu559Phe)	rs794728374
NM_000238.4(KCNH2):c.2246G>T (p.Gly749Val)	rs199472989
NM_000238.4(KCNH2):c.244_252dup (p.Gln84_Ala85insIleAlaGln)	rs794728476
NM_000238.4(KCNH2):c.2771G>A (p.Gly924Glu)	rs199473009
NM_000238.4(KCNH2):c.298C>G (p.Arg100Gly)	rs121912515

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