ClinVar Miner

Submissions for variant NM_014874.4(MFN2):c.1963A>G (p.Lys655Glu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Section for Clinical Neurogenetics,University of Tübingen RCV001030783 SCV001156092 uncertain significance Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2A2B 2019-08-01 no assertion criteria provided research

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