ClinVar Miner

Submissions for variant NM_017570.5(OPLAH):c.2722C>T (p.Pro908Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002908315 SCV003250393 benign 5-Oxoprolinase deficiency 2024-08-20 criteria provided, single submitter clinical testing

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