ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.-68-80C>T (rs577322036)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000163738 SCV000214313 likely benign Hereditary cancer-predisposing syndrome 2018-07-16 criteria provided, single submitter clinical testing Other data supporting benign classification;Seen in trans with a mutation or in homozygous state in individual without severe disease for that gene

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