List of variants in gene combination LOC126861897, MHRT, MYH7 reported as uncertain significance for Myosin storage myopathy

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

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.4872G>A (p.Glu1624=)	rs766561921	0.00003
NM_000257.4(MYH7):c.4908C>T (p.Ala1636=)	rs150241539	0.00002
NM_000257.4(MYH7):c.4659C>T (p.His1553=)	rs570079347	0.00001
NM_000257.4(MYH7):c.4816C>T (p.Arg1606Cys)	rs200530211	0.00001
NM_000257.4(MYH7):c.5026C>T (p.Arg1676Trp)	rs753115999	0.00001
NM_000257.4(MYH7):c.5030G>A (p.Arg1677His)	rs730880914	0.00001
NM_000257.4(MYH7):c.4691A>C (p.Glu1564Ala)
NM_000257.4(MYH7):c.4828G>A (p.Glu1610Lys)	rs730880810
NM_000257.4(MYH7):c.4953+6C>A	rs1892187663
NM_000257.4(MYH7):c.4978G>C (p.Ala1660Pro)	rs1892176969
NM_000257.4(MYH7):c.5087A>G (p.Glu1696Gly)	rs1892168471
NM_000257.4(MYH7):c.5173_5175del (p.Asn1725del)
NM_000257.4(MYH7):c.5208G>C (p.Gln1736His)	rs886050416

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