ClinVar Miner

Submissions for variant NM_001243133.2(NLRP3):c.1131A>G (p.Lys377=)

dbSNP: rs755556220
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001786733 SCV002028649 likely benign not provided 2021-05-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002544300 SCV003224017 likely benign Cryopyrin associated periodic syndrome 2023-08-04 criteria provided, single submitter clinical testing

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