List of variants in gene combination LOC114827851, MYH6 reported as benign by Ambry Genetics

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.411G>A (p.Glu137=)	rs2277474	0.22054
NM_002471.4(MYH6):c.393G>A (p.Leu131=)	rs17277970	0.06973
NM_002471.4(MYH6):c.166G>A (p.Gly56Arg)	rs28711516	0.06950
NM_002471.4(MYH6):c.399G>A (p.Val133=)	rs78891557	0.01343
NM_002471.4(MYH6):c.36G>A (p.Ala12=)	rs141014719	0.00487
NM_002471.4(MYH6):c.86G>A (p.Arg29Gln)	rs150574114	0.00455
NM_002471.4(MYH6):c.-5C>A	rs183611755	0.00438
NM_002471.4(MYH6):c.427C>A (p.Arg143=)	rs2277473

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