ClinVar Miner

Submissions for variant NM_213674.1(TPM2):c.640-215C>G (rs137853307)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000013283 SCV000033530 pathogenic Cap myopathy 2 2008-12-02 no assertion criteria provided literature only
TPM2 homepage - Leiden Muscular Dystrophy pages RCV000128687 SCV000172327 not provided not provided no assertion provided not provided

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