ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.357-13C>A

gnomAD frequency: 0.00001  dbSNP: rs1264489096
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001804489 SCV002052912 likely benign Cardiomyopathy 2023-11-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002074188 SCV002417835 likely benign Charcot-Marie-Tooth disease type 2 2023-06-02 criteria provided, single submitter clinical testing

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