ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1413C>G (p.Arg471=)

dbSNP: rs1572365626
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001186943 SCV001353558 likely benign Cardiomyopathy 2018-11-25 criteria provided, single submitter clinical testing
Invitae RCV001405617 SCV001607551 likely benign Charcot-Marie-Tooth disease type 2 2018-10-06 criteria provided, single submitter clinical testing
GeneDx RCV000932267 SCV001793936 likely benign not provided 2019-08-28 criteria provided, single submitter clinical testing

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