List of variants in gene combination LOC126861897, MHRT, MYH7 reported as benign for Cardiomyopathy

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.5106G>A (p.Ala1702=)	rs3729830	0.14676
NM_000257.4(MYH7):c.4716C>T (p.Ile1572=)	rs7140196	0.01334
NM_000257.4(MYH7):c.4788G>A (p.Ser1596=)	rs146858930	0.00277
NM_000257.4(MYH7):c.4806C>T (p.Asp1602=)	rs142034311	0.00098
NM_000257.4(MYH7):c.4974C>T (p.Asp1658=)	rs374289523	0.00010
NM_000257.4(MYH7):c.4659C>T (p.His1553=)	rs570079347	0.00002
NM_000257.4(MYH7):c.4671G>A (p.Lys1557=)	rs200601164	0.00001

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