ClinVar Miner

Submissions for variant NM_006096.4(NDRG1):c.1081C>G (p.Arg361Gly)

dbSNP: rs779065972
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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 RCV001173710 SCV001336824 uncertain significance Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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