ClinVar Miner

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:
ClinVar version:
Total variants with conflicting interpretations: 22
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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.1731G>C (p.Glu577Asp) rs75160168
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.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.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.4740A>C (p.Ala1580=) rs61730806
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.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.714T>C (p.Thr238=) rs8068729
NM_002472.3(MYH8):c.805+9C>T rs75468422

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