ClinVar Miner

Submissions for variant NM_002485.4(NBN):c.1398-10dup (rs587780555)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001080891 SCV000153974 benign Microcephaly, normal intelligence and immunodeficiency 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000160772 SCV000211431 benign Hereditary cancer-predisposing syndrome 2014-07-02 criteria provided, single submitter clinical testing The variant is found in HEREDICANCER,BR-OV-HEREDIC panel(s).
Genetic Services Laboratory,University of Chicago RCV000504209 SCV000595909 likely benign not specified 2016-06-07 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000504209 SCV000601672 benign not specified 2016-09-15 criteria provided, single submitter clinical testing
Color RCV000160772 SCV000685715 likely benign Hereditary cancer-predisposing syndrome 2015-04-24 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759887 SCV000889548 benign not provided 2016-09-15 criteria provided, single submitter clinical testing

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