List of variants in gene combination LOC114827851, MYH6 reported as likely benign for Cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.420C>T (p.Ala140=)	rs145023897	0.00010
NM_002471.4(MYH6):c.636G>A (p.Ala212=)	rs111265123	0.00003
NM_002471.4(MYH6):c.354G>A (p.Ser118=)	rs373427673	0.00002
NM_002471.4(MYH6):c.105T>C (p.Thr35=)	rs1345462210

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