ClinVar Miner

Submissions for variant NM_001366385.1(CARD14):c.2409G>A (p.Thr803=)

gnomAD frequency: 0.00638  dbSNP: rs115102551
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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 RCV000632895 SCV000754100 benign Pityriasis rubra pilaris; Psoriasis 2 2025-01-23 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002263854 SCV002543271 likely benign Autoinflammatory syndrome 2021-12-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710166 SCV005248820 benign not provided criteria provided, single submitter not provided

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