ClinVar Miner

Submissions for variant NM_001366385.1(CARD14):c.2807+10C>T

gnomAD frequency: 0.00019  dbSNP: rs368700533
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000907577 SCV001052293 benign Pityriasis rubra pilaris; Psoriasis 2 2024-01-25 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002264078 SCV002543291 likely benign Autoinflammatory syndrome 2021-10-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710208 SCV005248830 benign not provided criteria provided, single submitter not provided

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