ClinVar Miner

Submissions for variant NM_001081.3(CUBN):c.4964C>G (p.Pro1655Arg) (rs532968940)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000379950 SCV000361716 uncertain significance Megaloblastic anemia 2016-06-14 criteria provided, single submitter clinical testing
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare RCV000786895 SCV000925794 uncertain significance Megaloblastic anemia due to inborn errors of metabolism 2018-11-07 no assertion criteria provided clinical testing

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