Variants in gene combination MYH2, MYHAS with conflicting interpretations reported as "likely benign and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_017534.6(MYH2):c.2967A>G (p.Ala989=)	rs113190032	0.01110
NM_017534.6(MYH2):c.4329C>T (p.Ala1443=)	rs61739663	0.00465
NM_017534.6(MYH2):c.2908G>A (p.Val970Ile)	rs143872329	0.00456
NM_017534.6(MYH2):c.5780G>A (p.Arg1927Gln)	rs34161789	0.00444
NM_017534.6(MYH2):c.2295G>A (p.Gly765=)	rs79757188	0.00317
NM_017534.6(MYH2):c.3181C>G (p.Leu1061Val)	rs142586585	0.00225
NM_017534.6(MYH2):c.3432C>T (p.Asp1144=)	rs184725551	0.00091
NM_017534.6(MYH2):c.2106C>T (p.Asn702=)	rs145039915	0.00085
NM_017534.6(MYH2):c.2304+7T>G	rs370223713	0.00034
NM_017534.6(MYH2):c.3582A>G (p.Thr1194=)	rs200505060	0.00034

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