ClinVar Miner

Submissions for variant NM_014874.3(MFN2):c.723C>T (p.Phe241=) (rs764912025)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000206786 SCV000260943 likely benign not provided 2016-12-09 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001172994 SCV001336069 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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