List of variants in gene KCNH2 reported as likely pathogenic by Medical Research Institute, Tokyo Medical and Dental University

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.1831T>G (p.Tyr611Asp)	rs199472942
NM_000238.4(KCNH2):c.1849T>C (p.Phe617Leu)	rs796052195
NM_000238.4(KCNH2):c.307+2T>A	rs796052196

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