ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.-448G>A

gnomAD frequency: 0.09540  dbSNP: rs3136229
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074623 SCV000108206 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
GeneDx RCV001707520 SCV001935052 benign not provided 2019-01-10 criteria provided, single submitter clinical testing

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