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

Minimum submission review status:		Collection method:
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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.5287G>A (p.Ala1763Thr)	rs727504355	0.00009
NM_000257.4(MYH7):c.5243G>A (p.Cys1748Tyr)	rs200303340	0.00005
NM_000257.4(MYH7):c.5279C>T (p.Thr1760Met)	rs727505294	0.00001

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