List of variants in gene combination LOC126861897, MHRT, MYH7 reported as not provided for hereditary skeletal muscle disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.4679G>C (p.Arg1560Pro)	rs730880806
NM_000257.4(MYH7):c.4844AGA[2] (p.Lys1617del)	rs121913648
NM_000257.4(MYH7):c.5177AGA[3] (p.Lys1729del)	rs367543052

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