ClinVar Miner

Submissions for variant NM_001289104.2(PRKCSH):c.1071T>C (p.Pro357=)

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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 RCV002639224 SCV002978832 likely benign not provided 2023-02-15 criteria provided, single submitter clinical testing

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