ClinVar Miner

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

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 8
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NM_002472.3(MYH8):c.1209C>A (p.Cys403Ter) rs144321381
NM_002472.3(MYH8):c.2274A>G (p.Gln758=) rs145901155
NM_002472.3(MYH8):c.3340T>C (p.Leu1114=) rs142711931
NM_002472.3(MYH8):c.5293-1G>A rs144785726
NM_002472.3(MYH8):c.5350C>G (p.Arg1784Gly) rs141215006
NM_002472.3(MYH8):c.5464G>A (p.Val1822Ile) rs143876651
NM_002472.3(MYH8):c.578G>A (p.Arg193His) rs145863180
NM_002472.3(MYH8):c.675C>T (p.Ser225=) rs146651214

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