ClinVar Miner

Submissions for variant NM_001366385.1(CARD14):c.1170C>T (p.Phe390=)

gnomAD frequency: 0.03377  dbSNP: rs74951924
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000542164 SCV000629229 benign Pityriasis rubra pilaris; Psoriasis 2 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001564771 SCV001787984 likely benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002263742 SCV002543211 benign Autoinflammatory syndrome 2022-01-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001564771 SCV005214248 likely benign not provided criteria provided, single submitter not provided

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