ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.98606G>C (p.Arg32869Pro)

dbSNP: rs587780495
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000118795 SCV000153413 likely pathogenic Tibial muscular dystrophy 2013-10-07 criteria provided, single submitter clinical testing

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