List of variants in gene combination LOC126861897, MHRT, MYH7 reported by Genetics and Genomics Program, Sidra Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.4822C>T (p.Arg1608Cys)	rs746571601	0.00001
NM_000257.4(MYH7):c.5030G>A (p.Arg1677His)	rs730880914	0.00001
NM_000257.4(MYH7):c.4808C>T (p.Ala1603Val)	rs1892198053
NM_000257.4(MYH7):c.4985G>A (p.Arg1662His)	rs370328209

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