ClinVar Miner

Submissions for variant NM_012275.3(IL36RN):c.369G>C (p.Thr123=)

gnomAD frequency: 0.00682  dbSNP: rs28938778
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000635397 SCV000756808 benign Generalized pustular psoriasis 2024-01-31 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002263870 SCV002543491 likely benign Autoinflammatory syndrome 2019-11-01 criteria provided, single submitter clinical testing

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