ClinVar Miner

Submissions for variant NM_032415.7(CARD11):c.215G>T (p.Arg72Leu)

dbSNP: rs2115093887
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Washington Center for Mendelian Genomics, University of Washington RCV001543391 SCV001761949 likely pathogenic Immunodeficiency 11b with atopic dermatitis no assertion criteria provided research

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