ClinVar Miner

Submissions for variant NM_002617.4(PEX10):c.533A>G (p.His178Arg)

dbSNP: rs1643081768
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004587107 SCV005076754 uncertain significance not specified 2024-04-29 criteria provided, single submitter clinical testing
Natera, Inc. RCV001280060 SCV001467207 uncertain significance Zellweger spectrum disorders 2020-08-05 no assertion criteria provided clinical testing

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