ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.4002-9_4002-7del

dbSNP: rs864622105
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000205595 SCV000259344 uncertain significance Lynch syndrome 2015-07-08 criteria provided, single submitter clinical testing

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