Variants in gene combination MHRT, MYH7 with conflicting interpretations reported as "likely benign and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn)	rs201307101	0.00024
NM_000257.4(MYH7):c.4423C>T (p.Arg1475Cys)	rs139646545	0.00009
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=)	rs45560242	0.00008
NM_000257.4(MYH7):c.4399C>G (p.Leu1467Val)	rs397516214	0.00002
NM_000257.4(MYH7):c.4557C>T (p.Ser1519=)	rs150552664	0.00002
NM_000257.4(MYH7):c.4520-3C>T	rs549509054	0.00001
NM_000257.4(MYH7):c.4644+3G>A	rs397516226	0.00001
NM_000257.4(MYH7):c.4354-7C>T	rs370093487

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