List of variants in gene MYH7 reported as likely pathogenic by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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_000257.4(MYH7):c.1987C>A (p.Arg663Ser)	rs397516127
NM_000257.4(MYH7):c.2011C>T (p.Arg671Cys)	rs727503263
NM_000257.4(MYH7):c.2192C>G (p.Pro731Arg)	rs1247313340
NM_000257.4(MYH7):c.3613G>A (p.Glu1205Lys)	rs727505026
NM_000257.4(MYH7):c.5560-2A>C	rs1566521710

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