ClinVar Miner

Submissions for variant NM_000287.4(PEX6):c.2649A>G (p.Leu883=)

dbSNP: rs752553005
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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 RCV001490316 SCV001694877 likely benign Peroxisome biogenesis disorder 2019-09-22 criteria provided, single submitter clinical testing

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