ClinVar Miner

Submissions for variant NM_001199138.2(NLRC4):c.1098C>T (p.Phe366=)

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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 RCV003806923 SCV004594371 likely benign Periodic fever-infantile enterocolitis-autoinflammatory syndrome; Familial cold autoinflammatory syndrome 4 2023-09-14 criteria provided, single submitter clinical testing

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