ClinVar Miner

Submissions for variant NM_002485.4(NBN):c.267A>G (p.Arg89=) (rs1554568316)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000773654 SCV000907348 likely benign Hereditary cancer-predisposing syndrome 2015-04-02 criteria provided, single submitter clinical testing
Invitae RCV000558967 SCV000634291 likely benign Microcephaly, normal intelligence and immunodeficiency 2017-02-02 criteria provided, single submitter clinical testing

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