ClinVar Miner

Submissions for variant NM_012092.3(ICOS):c.40C>T (p.Arg14Cys) (rs77411896)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000508428 SCV000604007 benign not provided 2018-01-13 criteria provided, single submitter clinical testing
Invitae RCV001080790 SCV000769918 benign Common variable immunodeficiency 1 2019-12-31 criteria provided, single submitter clinical testing

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