ClinVar Miner

Submissions for variant NM_001199138.2(NLRC4):c.2615-8T>C

dbSNP: rs1553343121
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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 RCV000652412 SCV000774282 likely benign Periodic fever-infantile enterocolitis-autoinflammatory syndrome; Familial cold autoinflammatory syndrome 4 2019-12-31 criteria provided, single submitter clinical testing

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