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

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.3111C>T (p.Asp1037=)	rs200799870	0.00134
NM_000238.4(KCNH2):c.1563C>T (p.Ile521=)	rs143011005	0.00097
NM_000238.4(KCNH2):c.51C>G (p.Thr17=)	rs144338227	0.00083
NM_000238.4(KCNH2):c.442C>T (p.Arg148Trp)	rs139544114	0.00062
NM_000238.4(KCNH2):c.1039C>T (p.Pro347Ser)	rs138776684	0.00061
NM_000238.4(KCNH2):c.2729C>T (p.Pro910Leu)	rs199473436	0.00023
NM_000238.4(KCNH2):c.3164G>A (p.Arg1055Gln)	rs41307270	0.00004
NM_000238.4(KCNH2):c.3094C>T (p.Arg1032Trp)	rs373394254	0.00003
NM_000238.4(KCNH2):c.2331C>T (p.Thr777=)	rs41307292	0.00002
NM_000238.4(KCNH2):c.1320G>T (p.Pro440=)	rs144926928
NM_000238.4(KCNH2):c.2398+105del	rs546898924
NM_000238.4(KCNH2):c.3140G>T (p.Arg1047Leu)	rs36210421
NM_000238.4(KCNH2):c.551GCGCGGGCG[1] (p.184GAG[1])	rs551056698

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