List of variants in gene JPH2 reported as likely benign for Hypertrophic cardiomyopathy 17; Cardiomyopathy, dilated, 2E

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_020433.5(JPH2):c.1566G>A (p.Arg522=)	rs559143345	0.00031
NM_020433.5(JPH2):c.579C>T (p.Pro193=)	rs534491843	0.00014
NM_020433.5(JPH2):c.380-20C>T	rs779167207	0.00006

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