List of variants in gene combination LOC126861896, MYH6 reported as benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.4914T>C (p.Ala1638=)	rs178640	0.53346
NM_002471.4(MYH6):c.4651-17G>A	rs2071634	0.23331
NM_002471.4(MYH6):c.4980C>T (p.Asp1660=)	rs382872	0.07807
NM_002471.4(MYH6):c.4960-17A>T	rs28730764	0.03950
NM_002471.4(MYH6):c.4838T>C (p.Val1613Ala)	rs61742476	0.03922
NM_002471.4(MYH6):c.4778A>T (p.Gln1593Leu)	rs45574136	0.03900
NM_002471.4(MYH6):c.4959+13G>A	rs28730765	0.00762
NM_002471.4(MYH6):c.4651-12A>C	rs193922653	0.00413
NM_002471.4(MYH6):c.4986G>A (p.Ala1662=)	rs77416370	0.00066

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