ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.2163-18G>A

dbSNP: rs606231333
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002514596 SCV003010040 likely benign Hypertrophic cardiomyopathy 2022-01-03 criteria provided, single submitter clinical testing
Evolutionary and Medical Genetics Laboratory, Centre for Cellular and Molecular Biology RCV000148964 SCV000154213 unknown Familial cardiomyopathy no assertion criteria provided not provided Converted during submission to Uncertain significance.

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