ClinVar Miner

Submissions for variant NM_002661.5(PLCG2):c.1194-18A>G

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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 RCV002612394 SCV003514103 benign Familial cold autoinflammatory syndrome 3 2024-01-02 criteria provided, single submitter clinical testing

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