ClinVar Miner

Submissions for variant NM_014874.3(MFN2):c.292A>G (p.Lys98Glu) (rs1553141706)

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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 RCV000518242 SCV000614090 uncertain significance not specified 2016-09-12 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV000790050 SCV001337444 uncertain significance Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing
Inherited Neuropathy Consortium RCV000790050 SCV000929440 uncertain significance Charcot-Marie-Tooth disease no assertion criteria provided literature only

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