ClinVar Miner

Submissions for variant NM_000287.4(PEX6):c.1509T>C (p.Ser503=)

dbSNP: rs1268177698
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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 RCV001495090 SCV001699759 likely benign Peroxisome biogenesis disorder 2024-02-07 criteria provided, single submitter clinical testing

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