ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.4777-20A>G (rs3218678)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000130992 SCV000185915 benign Hereditary cancer-predisposing syndrome 2012-07-09 criteria provided, single submitter clinical testing
Color RCV000130992 SCV000537371 benign Hereditary cancer-predisposing syndrome 2015-04-01 criteria provided, single submitter clinical testing
Counsyl RCV000672214 SCV000797299 benign Ataxia-telangiectasia syndrome 2018-01-19 criteria provided, single submitter clinical testing
PreventionGenetics RCV000251780 SCV000301671 benign not specified criteria provided, single submitter clinical testing

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