ClinVar Miner

Submissions for variant NM_000287.4(PEX6):c.945T>C (p.Pro315=)

dbSNP: rs2150236089
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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 RCV002179670 SCV002335754 likely benign Peroxisome biogenesis disorder 2023-10-31 criteria provided, single submitter clinical testing

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