ClinVar Miner

Submissions for variant NM_000287.4(PEX6):c.1821C>A (p.Ala607=)

dbSNP: rs201730259
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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 RCV001409536 SCV001611565 likely benign Peroxisome biogenesis disorder 2023-12-01 criteria provided, single submitter clinical testing

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