ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.639+9T>C

dbSNP: rs745768694
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000788525 SCV000927674 uncertain significance not provided 2018-05-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001501103 SCV001705908 likely benign Charcot-Marie-Tooth disease type 2 2021-04-28 criteria provided, single submitter clinical testing

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