Variants in gene combination MYH8, MYHAS with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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
NM_002472.3(MYH8):c.1907C>T (p.Ala636Val)	rs34693726
NM_002472.3(MYH8):c.2016C>T (p.Phe672=)	rs12936716
NM_002472.3(MYH8):c.3117G>A (p.Gly1039=)	rs3744553
NM_002472.3(MYH8):c.3270C>T (p.Ile1090=)	rs3744552
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.5074T>C (p.Trp1692Arg)	rs8069834
NM_002472.3(MYH8):c.5208C>T (p.Asp1736=)	rs33969260
NM_002472.3(MYH8):c.5350C>G (p.Arg1784Gly)	rs141215006
NM_002472.3(MYH8):c.714T>C (p.Thr238=)	rs8068729

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