ClinVar Miner

Submissions for variant NM_000288.4(PEX7):c.634-9T>C

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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 RCV002645999 SCV002963693 likely benign Peroxisome biogenesis disorder 9B 2022-05-15 criteria provided, single submitter clinical testing

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