ClinVar Miner

Submissions for variant NM_152263.4(TPM3):c.*5028_*5029dup

dbSNP: rs886045291
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV001795891 SCV000348342 uncertain significance Congenital myopathy with fiber type disproportion 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000300424 SCV000348343 uncertain significance Nemaline myopathy 2016-06-14 criteria provided, single submitter clinical testing

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