ClinVar Miner

Submissions for variant NM_014874.4(MFN2):c.2070-11C>T

dbSNP: rs759614417
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory, London Health Sciences Centre RCV001172995 SCV001336070 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing
Invitae RCV002068071 SCV002375327 likely benign Charcot-Marie-Tooth disease type 2 2022-09-07 criteria provided, single submitter clinical testing

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