ClinVar Miner

Submissions for variant NM_001366385.1(CARD14):c.1098C>T (p.Ser366=)

gnomAD frequency: 0.00003  dbSNP: rs749480979
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001448889 SCV001651992 likely benign Pityriasis rubra pilaris; Psoriasis 2 2023-08-02 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002264323 SCV002543176 uncertain significance Autoinflammatory syndrome 2020-02-01 criteria provided, single submitter clinical testing

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