List of variants in gene combination LOC126861897, MHRT, MYH7 reported as benign 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: 3

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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	0.01445
NM_000257.4(MYH7):c.4806C>T (p.Asp1602=)	rs142034311	0.00098

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