List of variants in gene combination LOC126861897, MHRT, MYH7 reported as uncertain significance for Dilated cardiomyopathy 1S

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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.4909G>A (p.Ala1637Thr)	rs141122361	0.00034
NM_000257.4(MYH7):c.5020G>A (p.Val1674Met)	rs397516235	0.00002
NM_000257.4(MYH7):c.5096G>A (p.Arg1699Gln)	rs146778113	0.00002
NM_000257.4(MYH7):c.4717G>A (p.Glu1573Lys)	rs750987717	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.4681G>T (p.Ala1561Ser)
NM_000257.4(MYH7):c.4828G>A (p.Glu1610Lys)	rs730880810
NM_000257.4(MYH7):c.4901G>A (p.Arg1634His)	rs545875689
NM_000257.4(MYH7):c.4953+6C>A	rs1892187663
NM_000257.4(MYH7):c.5087A>G (p.Glu1696Gly)	rs1892168471
NM_000257.4(MYH7):c.5105C>A (p.Ala1702Glu)
NM_000257.4(MYH7):c.5208G>C (p.Gln1736His)	rs886050416

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