ClinVar Miner

Submissions for variant NM_006059.4(LAMC3):c.368G>T (p.Arg123Leu)

gnomAD frequency: 0.00284  dbSNP: rs140461419
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000883886 SCV000523082 likely benign not provided 2019-02-19 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000428109 SCV000595535 likely benign not specified 2015-12-31 criteria provided, single submitter clinical testing
Invitae RCV000883886 SCV001027224 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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