ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.1039-8_1039-7insTA (rs535965616)

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Total submissions: 8
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000160559 SCV000211138 benign Hereditary cancer-predisposing syndrome 2014-07-07 criteria provided, single submitter clinical testing The variant is found in HEREDICANCER,BR-OV-HEREDIC panel(s).
Invitae RCV000195736 SCV000253129 benign Hereditary nonpolyposis colorectal neoplasms 2020-11-21 criteria provided, single submitter clinical testing
Color Health, Inc RCV000160559 SCV001351740 likely benign Hereditary cancer-predisposing syndrome 2019-09-03 criteria provided, single submitter clinical testing
Institute of Human Genetics, University of Leipzig Medical Center RCV001262554 SCV001440475 likely benign Breast carcinoma 2019-01-01 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001529186 SCV001742227 likely benign not provided no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001529186 SCV001797325 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics,Academic Medical Center RCV001699048 SCV001922878 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001529186 SCV001927854 likely benign not provided no assertion criteria provided clinical testing

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