ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3173-35C>T

gnomAD frequency: 0.00070  dbSNP: rs186475107
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
Mendelics RCV000986732 SCV001135833 likely benign Lynch syndrome 5 2019-05-28 criteria provided, single submitter clinical testing

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