ClinVar Miner

Submissions for variant NM_173841.2(IL1RN):c.-95C>G

gnomAD frequency: 0.00007  dbSNP: rs1458187927
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002264630 SCV002543469 uncertain significance Autoinflammatory syndrome 2017-01-06 criteria provided, single submitter clinical testing

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