ClinVar Miner

Submissions for variant NM_001366385.1(CARD14):c.921G>A (p.Ser307=)

dbSNP: rs753922155
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001502903 SCV001707742 likely benign Pityriasis rubra pilaris; Psoriasis 2 2024-10-22 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002264358 SCV002543342 uncertain significance Autoinflammatory syndrome 2017-06-08 criteria provided, single submitter clinical testing

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