ClinVar Miner

Submissions for variant NM_006096.4(NDRG1):c.856-9C>T (rs772996128)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000886772 SCV001030299 likely benign not provided 2018-05-14 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001174336 SCV001337472 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing
Invitae RCV001424715 SCV001627315 likely benign Charcot-Marie-Tooth disease type 4 2018-05-14 criteria provided, single submitter clinical testing

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