ClinVar Miner

Submissions for variant NM_012275.3(IL36RN):c.381C>T (p.Ala127=)

gnomAD frequency: 0.00001  dbSNP: rs760489144
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002111898 SCV002399819 likely benign Generalized pustular psoriasis 2023-02-03 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002264460 SCV002543492 uncertain significance Autoinflammatory syndrome 2020-03-01 criteria provided, single submitter clinical testing

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