ClinVar Miner

Submissions for variant NM_006059.4(LAMC3):c.2516C>T (p.Thr839Met)

gnomAD frequency: 0.00893  dbSNP: rs57816762
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Total submissions: 5
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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 RCV000514984 SCV000610146 likely benign not provided 2017-02-22 criteria provided, single submitter clinical testing
Invitae RCV000514984 SCV001103541 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV000514984 SCV001857897 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV000514984 SCV001800496 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001726207 SCV001964822 benign not specified no assertion criteria provided clinical testing

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