Variants in gene combination MYH8, 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: 14

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HGVS	dbSNP
NM_002472.3(MYH8):c.1209C>A (p.Cys403Ter)	rs144321381
NM_002472.3(MYH8):c.1701G>A (p.Gln567=)	rs73275411
NM_002472.3(MYH8):c.2147T>A (p.Ile716Asn)	rs115483891
NM_002472.3(MYH8):c.225G>C (p.Arg75Ser)	rs146732664
NM_002472.3(MYH8):c.2432+6A>C	rs111692916
NM_002472.3(MYH8):c.3686T>C (p.Met1229Thr)	rs35962914
NM_002472.3(MYH8):c.4233C>T (p.Asn1411=)	rs138992963
NM_002472.3(MYH8):c.4740A>C (p.Ala1580=)	rs61730806
NM_002472.3(MYH8):c.5350C>G (p.Arg1784Gly)	rs141215006
NM_002472.3(MYH8):c.540C>T (p.Thr180=)	rs34613390
NM_002472.3(MYH8):c.5464G>A (p.Val1822Ile)	rs143876651
NM_002472.3(MYH8):c.5513A>C (p.Glu1838Ala)	rs111567318
NM_002472.3(MYH8):c.578G>A (p.Arg193His)	rs145863180
NM_002472.3(MYH8):c.805+9C>T	rs75468422

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