ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.885-81G>C

gnomAD frequency: 0.02021  dbSNP: rs104894999
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000075918 SCV000106937 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
GeneDx RCV000114849 SCV001881478 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Harris Lab, University of Minnesota RCV000114849 SCV000148744 not provided not provided no assertion provided not provided

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