ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1077-229C>T

gnomAD frequency: 0.00492  dbSNP: rs148883469
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001585496 SCV001819446 likely benign not provided 2019-02-04 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256823 SCV002528807 benign Hereditary cancer-predisposing syndrome 2021-05-17 criteria provided, single submitter curation

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