ClinVar Miner

Submissions for variant NM_001079866.2(BCS1L):c.132G>C (p.Arg44=)

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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 RCV003564328 SCV004316439 likely benign not provided 2023-09-03 criteria provided, single submitter clinical testing

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