ClinVar Miner

Submissions for variant NM_014271.4(IL1RAPL1):c.974AAG[1] (p.Glu326del)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Juno Genomics, Hangzhou Juno Genomics, Inc RCV004796467 SCV005418958 uncertain significance Intellectual disability, X-linked 21 criteria provided, single submitter clinical testing PM2_Supporting+PM4+PM6_Supporting+PP4

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