ClinVar Miner

Submissions for variant NM_014874.3(MFN2):c.2018T>C (p.Leu673Pro) (rs1569871653)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV001092580 SCV001249141 uncertain significance not provided 2019-10-01 criteria provided, single submitter clinical testing
Inherited Neuropathy Consortium RCV000790045 SCV000929435 uncertain significance Charcot-Marie-Tooth disease no assertion criteria provided literature only

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