List of variants in gene MYH6 studied for Hypertrophic cardiomyopathy 1

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.831G>T (p.Gln277His)	rs140660481	0.00026
NM_002471.4(MYH6):c.1753G>A (p.Gly585Ser)	rs150415679	0.00013
NM_002471.4(MYH6):c.4264C>T (p.Arg1422Trp)	rs200465713	0.00010
NM_002471.4(MYH6):c.2589G>C (p.Glu863Asp)	rs763692915	0.00001
NM_002471.4(MYH6):c.4241C>T (p.Ser1414Phe)	rs863225267	0.00001
NM_002471.4(MYH6):c.2091C>A (p.Cys697Ter)	rs1891418103
NM_002471.4(MYH6):c.3193dup (p.Gln1065fs)	rs863225269
NM_002471.4(MYH6):c.4645G>A (p.Ala1549Thr)	rs1342437470

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