List of variants in gene KCNH2 reported as benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.1956T>C (p.Tyr652=)	rs1137617	0.70278
NM_000238.4(KCNH2):c.1692A>G (p.Leu564=)	rs1805121	0.51247
NM_000238.4(KCNH2):c.1539C>T (p.Phe513=)	rs1805120	0.25427
NM_000238.4(KCNH2):c.2690A>C (p.Lys897Thr)	rs1805123	0.20300
NM_000238.4(KCNH2):c.1563C>T (p.Ile521=)	rs143011005	0.00097
NM_000238.4(KCNH2):c.1467C>T (p.Ile489=)	rs740952
NM_000238.4(KCNH2):c.2692+7C>G	rs372023163

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