List of variants in gene combination LOC126861896, 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.4782G>A (p.Arg1594=)	rs142823394	0.00125
NM_002471.4(MYH6):c.4695A>G (p.Leu1565=)	rs374702183	0.00005
NM_002471.4(MYH6):c.4983T>C (p.Asp1661=)	rs763573894	0.00003
NM_002471.4(MYH6):c.4665C>T (p.His1555=)	rs373888186

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