ClinVar Miner

Submissions for variant NM_002582.4(PARN):c.887_888del (p.Thr296fs)

dbSNP: rs1970309647
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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 RCV001034546 SCV001197911 likely pathogenic Pulmonary fibrosis; Familial Interstitial Pneumonia no assertion criteria provided research

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