ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.4285_4287del (p.Met1429del)

dbSNP: rs1892274161
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV003320242 SCV001428798 uncertain significance Myosin storage myopathy 2019-06-12 criteria provided, single submitter clinical testing

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