ClinVar Miner

Submissions for variant NM_002617.4(PEX10):c.489G>T (p.Ala163=)

dbSNP: rs767442631
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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 RCV001506823 SCV001711759 likely benign Peroxisome biogenesis disorder, complementation group 7 2020-09-09 criteria provided, single submitter clinical testing

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