ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.465-5C>T (rs567202367)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000130832 SCV000185729 likely benign Hereditary cancer-predisposing syndrome 2017-06-08 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Co-occurence with a mutation in another gene that clearly explains a proband's phenotype,Other data supporting benign classification
Invitae RCV000859279 SCV000253257 likely benign not provided 2018-12-02 criteria provided, single submitter clinical testing
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia RCV000199796 SCV000296921 uncertain significance Peutz-Jeghers syndrome 2015-10-30 criteria provided, single submitter clinical testing
Counsyl RCV000199796 SCV000489545 likely benign Peutz-Jeghers syndrome 2016-10-19 criteria provided, single submitter clinical testing
Color RCV000130832 SCV000686660 likely benign Hereditary cancer-predisposing syndrome 2017-04-11 criteria provided, single submitter clinical testing

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