ClinVar Miner

Submissions for variant NM_002485.4(NBN):c.384A>G (p.Leu128=) (rs587780782)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000123217 SCV000166522 likely benign not provided 2019-01-21 criteria provided, single submitter clinical testing
Ambry Genetics RCV000219664 SCV000273731 likely benign Hereditary cancer-predisposing syndrome 2015-01-30 criteria provided, single submitter clinical testing
Color RCV000219664 SCV000685782 likely benign Hereditary cancer-predisposing syndrome 2017-05-12 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV000587700 SCV000697968 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing

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