ClinVar Miner

Submissions for variant NM_005562.3(LAMC2):c.846A>G (p.Pro282=)

gnomAD frequency: 0.00001  dbSNP: rs769572484
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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 RCV001503191 SCV001708041 likely benign not provided 2023-12-28 criteria provided, single submitter clinical testing

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