ClinVar Miner

Submissions for variant NM_014874.4(MFN2):c.2093A>G (p.His698Arg)

dbSNP: rs1060501916
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory, London Health Sciences Centre RCV001174297 SCV001337428 uncertain significance Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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