ClinVar Miner

Submissions for variant NM_000287.4(PEX6):c.192C>A (p.Thr64=)

dbSNP: rs1310661091
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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 RCV002065875 SCV002471919 likely benign Peroxisome biogenesis disorder 2024-09-15 criteria provided, single submitter clinical testing

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