List of variants in gene MYH6 reported as benign by CeGaT Center for Human Genetics Tuebingen

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.2946G>A (p.Glu982=)	rs145274612	0.01048
NM_002471.4(MYH6):c.1989C>T (p.Asn663=)	rs28730774	0.00451
NM_002471.4(MYH6):c.1275C>T (p.Ile425=)	rs61742470	0.00232
NM_002471.4(MYH6):c.3883G>C (p.Glu1295Gln)	rs34935550	0.00217
NM_002471.4(MYH6):c.2928+5G>A	rs28730772	0.00172
NM_002471.4(MYH6):c.1763A>C (p.Asp588Ala)	rs142992009	0.00153
NM_002471.4(MYH6):c.3303G>A (p.Val1101=)	rs143825034	0.00095
NC_000014.9:g.23409719C>A

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