ClinVar Miner

Submissions for variant NM_014845.5(FIG4):c.2154A>G (p.Pro718=) (rs201138266)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001088800 SCV000657856 likely benign Charcot-Marie-Tooth disease type 4 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000534342 SCV001154850 uncertain significance not provided 2016-07-01 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173285 SCV001336368 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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