ClinVar Miner

Submissions for variant NM_000057.4(BLM):c.2824-473C>T (rs28385070)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Washington Department of Laboratory Medicine,University of Washington RCV000209159 SCV000264966 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing

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