ClinVar Miner

Submissions for variant NM_006096.4(NDRG1):c.856-5C>T

dbSNP: rs767437478
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000868032 SCV001009317 likely benign Charcot-Marie-Tooth disease type 4 2022-09-12 criteria provided, single submitter clinical testing

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