ClinVar Miner

Submissions for variant NM_007289.4(MME):c.1574A>C (p.Lys525Thr)

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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, Uniklinik RWTH Aachen RCV001248810 SCV001337693 uncertain significance Charcot-Marie-Tooth disease, axonal, type 2T criteria provided, single submitter clinical testing

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