ClinVar Miner

Submissions for variant NM_001258281.1(MSH2):c.-87G>A (rs552303079)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000129430 SCV000184200 likely benign Hereditary cancer-predisposing syndrome 2017-12-22 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Other data supporting benign classification,Subpopulation frequency in support of benign classification,Co-occurence with mutation in same gene (phase unknown)
Illumina Clinical Services Laboratory,Illumina RCV000364089 SCV000430905 uncertain significance Lynch syndrome 2016-06-14 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000507430 SCV000601488 uncertain significance not specified 2017-01-17 criteria provided, single submitter clinical testing

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