ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1356C>A (p.Val452=)

dbSNP: rs1572364681
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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 RCV001523911 SCV001733647 likely benign Cardiomyopathy 2020-08-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002568048 SCV003031852 likely benign Charcot-Marie-Tooth disease type 2 2021-12-12 criteria provided, single submitter clinical testing

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