ClinVar Miner

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:
ClinVar version:
Total variants with conflicting interpretations: 14
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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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