ClinVar Miner

Submissions for variant NM_014874.4(MFN2):c.1039-9G>T

dbSNP: rs1569853844
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001500161 SCV001704943 likely benign Charcot-Marie-Tooth disease type 2 2018-05-21 criteria provided, single submitter clinical testing

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