ClinVar Miner

Submissions for variant NM_005560.6(LAMA5):c.8655C>T (p.Phe2885=)

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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 RCV002765582 SCV003009555 likely benign not provided 2022-07-23 criteria provided, single submitter clinical testing

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