ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.10287G>A (p.Gln3429=)

gnomAD frequency: 0.00001  dbSNP: rs566428134
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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 RCV002539085 SCV001012088 benign Imerslund-Grasbeck syndrome 2024-10-21 criteria provided, single submitter clinical testing

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