ClinVar Miner

Submissions for variant NM_002857.4(PEX19):c.70+9_70+10insCGCT

dbSNP: rs777854895
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000732614 SCV000860589 uncertain significance not provided 2018-04-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067135 SCV002388211 likely benign Peroxisome biogenesis disorder 12A (Zellweger) 2025-01-03 criteria provided, single submitter clinical testing

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