ClinVar Miner

Submissions for variant NM_006096.4(NDRG1):c.766C>T (p.Leu256=)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory,London Health Sciences Centre RCV001174343 SCV001337479 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing
Invitae RCV001279783 SCV001596948 likely benign Charcot-Marie-Tooth disease type 4 2019-07-19 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279783 SCV001466911 uncertain significance Charcot-Marie-Tooth disease type 4 2020-10-13 no assertion criteria provided clinical testing

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