ClinVar Miner

Submissions for variant NM_014874.4(MFN2):c.404G>T (p.Arg135Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein RCV002291101 SCV002583337 uncertain significance Neuropathy, hereditary motor and sensory, type 6A 2021-11-02 no assertion criteria provided clinical testing

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