ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.885G>A (p.Ser295=) (rs776999079)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000864955 SCV001005847 likely benign Charcot-Marie-Tooth disease, type 2 2019-12-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001000647 SCV001157671 likely benign not specified 2019-01-23 criteria provided, single submitter clinical testing
Color RCV001176530 SCV001340547 likely benign Cardiomyopathy 2018-10-22 criteria provided, single submitter clinical testing

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