List of variants in gene combination MYH2, MYHAS reported as likely pathogenic by GeneDx

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_017534.6(MYH2):c.326G>A (p.Arg109His)	rs1468175087	0.00002
NM_017534.6(MYH2):c.1975-1G>C	rs201082272	0.00001
NM_017534.6(MYH2):c.1147+1G>T	rs1057518398
NM_017534.6(MYH2):c.3502G>T (p.Glu1168Ter)	rs765529429
NM_017534.6(MYH2):c.5594_5597del (p.Lys1865fs)	rs1567726515

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