ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.141C>T (p.Asp47=)

dbSNP: rs1649715628
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001451238 SCV001654865 likely benign Charcot-Marie-Tooth disease type 2 2024-09-23 criteria provided, single submitter clinical testing

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