ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3556+160T>C

gnomAD frequency: 0.03454  dbSNP: rs56320267
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) RCV000074879 SCV000108091 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
GeneDx RCV001650890 SCV001865599 benign not provided 2019-08-07 criteria provided, single submitter clinical testing

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