ClinVar Miner

Submissions for variant NM_002340.6(LSS):c.1455T>C (p.Asp485=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003440612 SCV004151986 likely benign not provided 2023-02-01 criteria provided, single submitter clinical testing LSS: BP4, BP7
Labcorp Genetics (formerly Invitae), Labcorp RCV003440612 SCV005798988 likely benign not provided 2024-09-05 criteria provided, single submitter clinical testing

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