ClinVar Miner

Submissions for variant NM_002617.4(PEX10):c.776+33G>T

gnomAD frequency: 0.38841  dbSNP: rs3795269
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001537788 SCV001754746 benign Peroxisome biogenesis disorder 6A (Zellweger) 2021-07-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001537789 SCV001754747 benign Peroxisome biogenesis disorder 6B 2021-07-08 criteria provided, single submitter clinical testing
GeneDx RCV001709728 SCV001936848 benign not provided 2018-08-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001709728 SCV005285692 benign not provided criteria provided, single submitter not provided

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