ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.-159C>T

gnomAD frequency: 0.07535  dbSNP: rs41540312
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) RCV000074619 SCV000107871 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
Illumina Laboratory Services, Illumina RCV000074619 SCV000483934 likely benign Lynch syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001618241 SCV001842689 benign not provided 2018-06-23 criteria provided, single submitter clinical testing

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