ClinVar Miner

Submissions for variant NM_001289104.2(PRKCSH):c.939GGA[11] (p.Glu325dup)

dbSNP: rs3217229
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001659603 SCV001881921 benign not provided 2020-05-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001659603 SCV002487123 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV003151345 SCV003839923 likely benign not specified 2022-12-19 no assertion criteria provided clinical testing

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