ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1323C>A (p.Ala441=)

dbSNP: rs140194535
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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 RCV001473180 SCV001677325 likely benign Charcot-Marie-Tooth disease type 2 2022-11-07 criteria provided, single submitter clinical testing

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