ClinVar Miner

Submissions for variant NM_000466.3(PEX1):c.473-7T>C

dbSNP: rs1792881897
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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 RCV001474280 SCV001678449 likely benign Zellweger spectrum disorders 2024-05-01 criteria provided, single submitter clinical testing

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