ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.937-11C>A

dbSNP: rs267607645
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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 RCV001182360 SCV001347794 likely benign Cardiomyopathy 2018-11-23 criteria provided, single submitter clinical testing
Invitae RCV002559022 SCV002998631 likely benign Charcot-Marie-Tooth disease type 2 2022-02-12 criteria provided, single submitter clinical testing

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