ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.838A>G (p.Ser280Gly)

dbSNP: rs1558659442
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000708858 SCV000837872 uncertain significance Lynch syndrome 2018-07-02 criteria provided, single submitter clinical testing
Mendelics RCV000986710 SCV001135796 uncertain significance Lynch syndrome 5 2019-05-28 criteria provided, single submitter clinical testing

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