ClinVar Miner

Submissions for variant NM_006059.4(LAMC3):c.2439C>G (p.Ser813Arg)

dbSNP: rs61637370
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000513693 SCV000609794 likely benign not provided 2017-02-22 criteria provided, single submitter clinical testing
Invitae RCV000513693 SCV001103540 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000513693 SCV001769584 likely benign not provided 2021-06-22 criteria provided, single submitter clinical testing

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