ClinVar Miner

Submissions for variant NM_005562.3(LAMC2):c.2080C>T (p.Arg694Cys)

gnomAD frequency: 0.00003  dbSNP: rs202038614
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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 RCV000925933 SCV001071488 likely benign not provided 2024-03-18 criteria provided, single submitter clinical testing

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