ClinVar Miner

Submissions for variant NM_001351132.2(PEX5):c.1182-6A>T

dbSNP: rs1945095734
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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 RCV001506652 SCV001711580 likely benign Peroxisome biogenesis disorder 2B 2025-01-27 criteria provided, single submitter clinical testing

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