ClinVar Miner

Submissions for variant NM_002661.5(PLCG2):c.867+12G>A

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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 RCV003051106 SCV003450328 benign Familial cold autoinflammatory syndrome 3 2024-01-17 criteria provided, single submitter clinical testing

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