List of variants in gene combination LOC114827851, MYH6 reported as benign by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.399G>A (p.Val133=)	rs78891557	0.01343
NM_002471.4(MYH6):c.330G>A (p.Ala110=)	rs77679218	0.00490
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.622G>A (p.Asp208Asn)	rs142027794	0.00415
NM_002471.4(MYH6):c.408C>T (p.Ala136=)	rs140732380	0.00024
NM_002471.4(MYH6):c.70C>A (p.Leu24Ile)	rs573489857

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