ClinVar Miner

Submissions for variant NM_001351132.2(PEX5):c.551+13A>C

gnomAD frequency: 0.00004  dbSNP: rs372527455
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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 RCV002108650 SCV002435567 likely benign Peroxisome biogenesis disorder 2B 2023-09-13 criteria provided, single submitter clinical testing

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