ClinVar Miner

Submissions for variant NM_005807.6(PRG4):c.3905_3909del (p.Arg1302fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV004764587 SCV005374123 likely pathogenic Camptodactyly-arthropathy-coxa vara-pericarditis syndrome 2024-09-22 criteria provided, single submitter clinical testing

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