ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1737C>T (p.Tyr579=)

dbSNP: rs2528027300
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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 RCV003532566 SCV004359131 likely benign Cardiomyopathy 2024-01-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005100360 SCV005800281 likely benign Charcot-Marie-Tooth disease type 2 2024-07-06 criteria provided, single submitter clinical testing

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