ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.6573-16A>G (rs764506673)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000245922 SCV000301681 likely benign not specified criteria provided, single submitter clinical testing
Color RCV000582287 SCV000687714 likely benign Hereditary cancer-predisposing syndrome 2016-06-20 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000679138 SCV000805604 likely benign not provided 2015-07-27 criteria provided, single submitter clinical testing

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