ClinVar Miner

Submissions for variant NM_002485.4(NBN):c.1914+9C>T (rs13312938)

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000131005 SCV000185931 benign Hereditary cancer-predisposing syndrome 2012-08-07 criteria provided, single submitter clinical testing
Color RCV000131005 SCV000685743 benign Hereditary cancer-predisposing syndrome 2015-04-06 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000119107 SCV000475291 likely benign Microcephaly, normal intelligence and immunodeficiency 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000119107 SCV000153818 benign Microcephaly, normal intelligence and immunodeficiency 2018-01-25 criteria provided, single submitter clinical testing
PreventionGenetics RCV000507886 SCV000806423 benign not specified 2016-11-22 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000507886 SCV000601680 benign not specified 2016-09-22 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759170 SCV000888330 benign not provided 2016-09-22 criteria provided, single submitter clinical testing

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