ClinVar Miner

Submissions for variant NM_001081.3(CUBN):c.4921del (p.Tyr1641fs) (rs1564443979)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare RCV000735732 SCV000863885 likely pathogenic Imerslund-Gräsbeck syndrome 2018-05-22 no assertion criteria provided clinical testing

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