ClinVar Miner

Submissions for variant NM_001351834.2(ATM):c.3403-13dup (rs3218681)

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Total submissions: 8
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000159614 SCV000183913 benign Hereditary cancer-predisposing syndrome 2012-12-18 criteria provided, single submitter clinical testing
Color RCV000159614 SCV000682128 benign Hereditary cancer-predisposing syndrome 2015-03-31 criteria provided, single submitter clinical testing
Color RCV000159614 SCV000687474 benign Hereditary cancer-predisposing syndrome 2015-04-26 criteria provided, single submitter clinical testing
GeneDx RCV000159614 SCV000209599 benign Hereditary cancer-predisposing syndrome 2014-01-31 criteria provided, single submitter clinical testing The variant is found in HEREDICANCER,BR-OV-HEREDIC,COLO-HEREDIC panel(s).
Genetic Services Laboratory, University of Chicago RCV000192572 SCV000246616 likely benign not specified 2015-07-29 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000286085 SCV000367047 benign Ataxia-telangiectasia syndrome 2016-06-14 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000192572 SCV000538365 benign not specified 2016-03-28 criteria provided, single submitter clinical testing Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency
PreventionGenetics RCV000192572 SCV000301662 benign not specified criteria provided, single submitter clinical testing

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