ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.-210C>T

gnomAD frequency: 0.00543  dbSNP: rs181096360
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074621 SCV000107925 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%

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