ClinVar Miner

Submissions for variant NM_014874.3(MFN2):c.467G>T (p.Ser156Ile) (rs1557521949)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000711276 SCV000841612 uncertain significance not provided 2018-01-30 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV000790014 SCV001337429 uncertain significance Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing
Inherited Neuropathy Consortium RCV000790014 SCV000929404 uncertain significance Charcot-Marie-Tooth disease no assertion criteria provided literature only

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