ClinVar Miner

Submissions for variant NM_004813.4(PEX16):c.113-6C>A

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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 RCV003841220 SCV004694663 likely benign Peroxisome biogenesis disorder 2023-08-04 criteria provided, single submitter clinical testing

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