ClinVar Miner

Submissions for variant NM_006059.4(LAMC3):c.4146G>A (p.Arg1382=)

dbSNP: rs147092908
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000906084 SCV000728631 likely benign not provided 2020-02-25 criteria provided, single submitter clinical testing
Invitae RCV000906084 SCV001050706 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000906084 SCV004032888 likely benign not provided 2024-01-01 criteria provided, single submitter clinical testing LAMC3: BP4, BS1

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