List of variants in gene MYH6 reported as uncertain significance by Baylor Genetics

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.3230A>T (p.Gln1077Leu)	rs377716628	0.00032
NM_002471.4(MYH6):c.1753G>A (p.Gly585Ser)	rs150415679	0.00014
NM_002471.4(MYH6):c.1088T>C (p.Met363Thr)	rs150272218	0.00003
NM_002471.4(MYH6):c.2615G>A (p.Arg872His)	rs773162706	0.00003
NM_002471.4(MYH6):c.1411-12T>C	rs749244720	0.00001
NM_002471.4(MYH6):c.1578G>C (p.Glu526Asp)	rs753062079	0.00001
NM_002471.4(MYH6):c.1482G>A (p.Met494Ile)	rs1891561643
NM_002471.4(MYH6):c.3946G>A (p.Asp1316Asn)
NM_002471.4(MYH6):c.4047C>A (p.Tyr1349Ter)	rs570555040
NM_002471.4(MYH6):c.5452G>C (p.Glu1818Gln)	rs201494081
NM_002471.4(MYH6):c.864C>G (p.Tyr288Ter)	rs186265521

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