ClinVar Miner

Submissions for variant NM_000287.4(PEX6):c.921A>C (p.Gly307=)

dbSNP: rs1770229227
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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 RCV001464217 SCV001668183 likely benign Peroxisome biogenesis disorder 2019-12-27 criteria provided, single submitter clinical testing

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