ClinVar Miner

Submissions for variant NM_001366385.1(CARD14):c.2885G>A (p.Arg962Gln)

gnomAD frequency: 0.04584  dbSNP: rs34850974
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000533370 SCV000629248 benign Pityriasis rubra pilaris; Psoriasis 2 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV001613342 SCV001836295 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002263757 SCV002543297 benign Autoinflammatory syndrome 2022-02-04 criteria provided, single submitter clinical testing

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