List of variants in gene combination LOC114827851, MYH6 reported as uncertain significance 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.292G>A (p.Glu98Lys)	rs140596256	0.00030
NM_002471.4(MYH6):c.642+1G>C	rs199989693	0.00001
NM_002471.4(MYH6):c.68G>A (p.Arg23His)	rs771786844	0.00001
NM_002471.4(MYH6):c.503-8T>C	rs1566516373
NM_002471.4(MYH6):c.601A>G (p.Ile201Val)	rs1891728161
NM_002471.4(MYH6):c.642+3G>A	rs374013248

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