List of variants in gene MYH6 reported as benign by PreventionGenetics, part of Exact Sciences

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.800-11A>G	rs434273	0.81807
NM_002471.4(MYH6):c.4526-34T>C	rs178642	0.47911
NM_002471.4(MYH6):c.4359+13C>T	rs8022522	0.46131
NM_002471.4(MYH6):c.3302T>C (p.Val1101Ala)	rs365990	0.44987
NM_002471.4(MYH6):c.2292+18C>T	rs452036	0.42619
NM_002471.4(MYH6):c.1962+39T>C	rs412768	0.35458
NM_002471.4(MYH6):c.1582-39C>T	rs439735	0.22818
NM_002471.4(MYH6):c.5565+22A>G	rs8006357	0.22619
NM_002471.4(MYH6):c.3388G>A (p.Ala1130Thr)	rs28730771	0.08821
NM_002471.4(MYH6):c.5598A>G (p.Leu1866=)	rs17091278	0.08756
NM_002471.4(MYH6):c.4011G>A (p.Ser1337=)	rs451794	0.07834
NM_002471.4(MYH6):c.5164-22A>G	rs178637	0.07783
NM_002471.4(MYH6):c.5259C>T (p.Ala1753=)	rs8004990	0.07782
NM_002471.4(MYH6):c.1335C>T (p.Asn445=)	rs61731179	0.03984
NM_002471.4(MYH6):c.999C>T (p.Thr333=)	rs78107039	0.03596
NM_002471.4(MYH6):c.4527G>A (p.Glu1509=)	rs34855944	0.02632
NM_002471.4(MYH6):c.2151C>T (p.Tyr717=)	rs76202964	0.01414
NM_002471.4(MYH6):c.1989C>T (p.Asn663=)	rs28730774	0.00451
NM_002471.4(MYH6):c.4395G>A (p.Ser1465=)	rs74039310	0.00368
NM_002471.4(MYH6):c.2071G>A (p.Val691Ile)	rs148915045	0.00284
NM_002471.4(MYH6):c.5400C>T (p.Asp1800=)	rs144329079	0.00141
NM_002471.4(MYH6):c.1122G>A (p.Ala374=)	rs148091079	0.00116
NM_002471.4(MYH6):c.5652C>T (p.Ala1884=)	rs200662317	0.00062
NM_002471.4(MYH6):c.5439G>A (p.Gln1813=)	rs200854143	0.00002
NM_002471.4(MYH6):c.3979-8del	rs193922652
NM_002471.4(MYH6):c.3979-9C>A	rs57660219
NM_002471.4(MYH6):c.3979-9C>G	rs57660219
NM_002471.4(MYH6):c.4360-7C>T	rs58949384

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