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

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 7

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HGVS	dbSNP
NM_000257.4(MYH7):c.1987C>A (p.Arg663Ser)
NM_000257.4(MYH7):c.2011C>T (p.Arg671Cys)	rs727503263
NM_000257.4(MYH7):c.2192C>G (p.Pro731Arg)
NM_000257.4(MYH7):c.2572C>T (p.Arg858Cys)	rs2754158
NM_000257.4(MYH7):c.2631G>T (p.Met877Ile)	rs1060505018
NM_000257.4(MYH7):c.3613G>A (p.Glu1205Lys)	rs727505026
NM_000257.4(MYH7):c.5560-2A>C	rs1566521710

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