ClinVar Miner

Submissions for variant NM_006096.4(NDRG1):c.756-5_756-4delinsTG

dbSNP: rs1855782584
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory, London Health Sciences Centre RCV001173725 SCV001336839 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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