ClinVar Miner

Submissions for variant NM_002485.4(NBN):c.621T>C (p.Ser207=) (rs876658177)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000219310 SCV000273087 likely benign Hereditary cancer-predisposing syndrome 2014-11-25 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV000587744 SCV000697974 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing
Invitae RCV000636803 SCV000758244 likely benign Microcephaly, normal intelligence and immunodeficiency 2017-11-16 criteria provided, single submitter clinical testing

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