ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.1101G>T (p.Lys367Asn) (rs606231318)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Evolutionary and Medical Genetics Laboratory, Centre for Cellular and Molecular Biology RCV000148980 SCV000154229 probable-pathogenic Familial cardiomyopathy no assertion criteria provided not provided Converted during submission to Likely pathogenic.

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