ClinVar Miner

Submissions for variant NM_001351132.2(PEX5):c.1394+18C>T

dbSNP: rs148648526
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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 RCV002208018 SCV002376660 likely benign Peroxisome biogenesis disorder 2B 2022-02-09 criteria provided, single submitter clinical testing

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