ClinVar Miner

Submissions for variant NM_005142.3(CBLIF):c.661G>A (p.Gly221Arg)

dbSNP: rs1590859406
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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 RCV001029986 SCV001192788 likely pathogenic Hereditary intrinsic factor deficiency 2019-10-08 no assertion criteria provided clinical testing

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