ClinVar Miner

Submissions for variant NM_014874.4(MFN2):c.1872+17G>T

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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 RCV005203930 SCV005841572 likely benign Charcot-Marie-Tooth disease type 2 2024-11-11 criteria provided, single submitter clinical testing

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