ClinVar Miner

Submissions for variant NM_002857.3(PEX19):c.261C>T (p.Phe87=) (rs146644725)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000288367 SCV000336515 likely benign not specified 2015-10-23 criteria provided, single submitter clinical testing
Invitae RCV000650590 SCV000772437 benign Peroxisome biogenesis disorder 12A 2017-08-30 criteria provided, single submitter clinical testing

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