List of variants in gene combination LOC126861896, MYH6 reported 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
		ClinVar version:

Total variants: 15

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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
NM_002471.4(MYH6):c.4905C>T (p.Asn1635=)	rs143048583	0.00043
NM_002471.4(MYH6):c.5140C>A (p.Arg1714=)	rs140651265	0.00036
NM_002471.4(MYH6):c.5112G>A (p.Ala1704=)	rs150450178	0.00031
NM_002471.4(MYH6):c.4651-3C>A	rs572175190	0.00009
NM_002471.4(MYH6):c.4959+12C>T	rs371661383	0.00003
NM_002471.4(MYH6):c.4685G>A (p.Arg1562Gln)	rs371068881	0.00002

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