ClinVar Miner

Submissions for variant NM_002485.4(NBN):c.2235-12C>T (rs1554553904)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000667854 SCV000792365 likely benign Microcephaly, normal intelligence and immunodeficiency 2017-06-20 criteria provided, single submitter clinical testing
Color RCV000772976 SCV000906358 likely benign Hereditary cancer-predisposing syndrome 2019-09-06 criteria provided, single submitter clinical testing

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