ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.4104G>T (p.Val1368=)

dbSNP: rs1480495431
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001454355 SCV001658078 likely benign Imerslund-Grasbeck syndrome 2019-05-15 criteria provided, single submitter clinical testing

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