ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1077-259G>T

gnomAD frequency: 0.01331  dbSNP: rs2347793
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
GeneDx RCV001581039 SCV001817728 likely benign not provided 2018-07-14 criteria provided, single submitter clinical testing

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