List of variants in gene combination LOC126861897, MYH7 reported as likely benign by All of Us Research Program, National Institutes of Health

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.5253T>C (p.Ala1751=)	rs776282574	0.00004
NM_000257.4(MYH7):c.5229G>A (p.Glu1743=)	rs149509691
NM_000257.4(MYH7):c.5265C>A (p.Ala1755=)	rs2138639281

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