ClinVar Miner

Submissions for variant NM_001184.4(ATR):c.7761+375C>T

gnomAD frequency: 0.00978  dbSNP: rs11717703
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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 RCV000208906 SCV000264911 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing

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