ClinVar Miner

Submissions for variant NM_006231.4(POLE):c.2869_2870del (p.Ala957fs)

dbSNP: rs1593776393
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000988946 SCV001138883 uncertain significance Colorectal cancer, susceptibility to, 12 2019-05-28 criteria provided, single submitter clinical testing

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