List of variants in gene MYH6 reported as uncertain significance for Hypertrophic cardiomyopathy

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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: 18

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.4328C>A (p.Ala1443Asp)	rs727503234	0.00019
NM_002471.4(MYH6):c.3195G>C (p.Gln1065His)	rs267606904	0.00015
NM_002471.4(MYH6):c.1132G>A (p.Gly378Ser)	rs148962966	0.00014
NM_002471.4(MYH6):c.3604G>A (p.Val1202Met)	rs368451573	0.00008
NM_002471.4(MYH6):c.3476C>T (p.Thr1159Met)	rs780305056	0.00004
NM_002471.4(MYH6):c.2827C>T (p.Arg943Cys)	rs368912844	0.00003
NM_002471.4(MYH6):c.1822G>A (p.Ala608Thr)	rs886050409	0.00002
NM_002471.4(MYH6):c.934G>A (p.Ala312Thr)	rs748143404	0.00002
NM_002471.4(MYH6):c.3220G>A (p.Asp1074Asn)	rs375169402	0.00001
NM_002471.4(MYH6):c.5645G>A (p.Arg1882His)	rs199755234	0.00001
NM_002471.4(MYH6):c.1551C>A (p.Asp517Glu)	rs757410478
NM_002471.4(MYH6):c.2904G>T (p.Lys968Asn)
NM_002471.4(MYH6):c.3979-8del	rs193922652
NM_002471.4(MYH6):c.3979-8dup	rs193922652
NM_002471.4(MYH6):c.4354G>A (p.Asp1452Asn)
NM_002471.4(MYH6):c.5320G>C (p.Glu1774Gln)
NM_002471.4(MYH6):c.5687C>T (p.Ser1896Phe)	rs1209697861
NM_002471.4(MYH6):c.675C>T (p.Asn225=)	rs886050413

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