ClinVar Miner

Submissions for variant NM_001366385.1(CARD14):c.1323C>T (p.Asp441=)

gnomAD frequency: 0.10192  dbSNP: rs11658460
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001516550 SCV001724846 benign Pityriasis rubra pilaris; Psoriasis 2 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001619920 SCV001844593 benign not provided 2018-07-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001619920 SCV005248791 benign not provided criteria provided, single submitter not provided

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