ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1534C>T (p.Leu512=)

dbSNP: rs2102895384
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001445038 SCV001648058 likely benign Charcot-Marie-Tooth disease type 2 2019-06-20 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003331157 SCV004038710 likely benign not specified 2023-08-19 criteria provided, single submitter clinical testing

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