ClinVar Miner

Submissions for variant NM_000466.3(PEX1):c.2556C>T (p.Leu852=)

dbSNP: rs2484659921
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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 RCV003593726 SCV004316718 likely benign Zellweger spectrum disorders 2024-01-04 criteria provided, single submitter clinical testing

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