ClinVar Miner

Submissions for variant NM_002617.4(PEX10):c.913-9T>C

dbSNP: rs1642980853
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001465145 SCV001669128 likely benign Peroxisome biogenesis disorder, complementation group 7 2019-12-15 criteria provided, single submitter clinical testing
Natera, Inc. RCV001280058 SCV001467205 uncertain significance Zellweger spectrum disorders 2020-08-17 no assertion criteria provided clinical testing

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