ClinVar Miner

Submissions for variant NM_005562.3(LAMC2):c.2569C>A (p.Arg857=)

dbSNP: rs780621237
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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 RCV002100812 SCV002389758 likely benign not provided 2021-11-02 criteria provided, single submitter clinical testing

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