ClinVar Miner

Submissions for variant NM_002661.5(PLCG2):c.1935-14G>T

dbSNP: rs55645129
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001810715 SCV001477898 benign not provided 2023-09-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001519488 SCV001728367 benign Familial cold autoinflammatory syndrome 3 2024-01-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001810715 SCV005253058 benign not provided criteria provided, single submitter not provided

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