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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