ClinVar Miner

Submissions for variant NM_006254.4(PRKCD):c.889-11T>C

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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 RCV002716197 SCV003005418 likely benign Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD 2022-03-03 criteria provided, single submitter clinical testing

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