ClinVar Miner

Submissions for variant NM_001258281.1(MSH2):c.744+25_744+29del (rs11309117)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia RCV000239020 SCV000296896 benign Lynch syndrome 2015-11-11 criteria provided, single submitter clinical testing
Invitae RCV000860492 SCV001000557 benign not provided 2019-03-04 criteria provided, single submitter clinical testing
Mendelics RCV000986658 SCV001135714 likely benign Lynch syndrome I 2019-05-28 criteria provided, single submitter clinical testing
Institute of Human Genetics, University of Leipzig Medical Center RCV000986658 SCV001429073 uncertain significance Lynch syndrome I 2018-07-09 criteria provided, single submitter clinical testing

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