ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1661+90T>C

gnomAD frequency: 0.03147  dbSNP: rs10183143
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) RCV000076220 SCV000107238 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
GeneDx RCV001537491 SCV001754378 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000202001 SCV000257147 benign not specified no assertion criteria provided research

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