ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.946_954del (p.Phe316_His318del)

dbSNP: rs1575509703
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987160 SCV001136391 uncertain significance Colorectal cancer, hereditary nonpolyposis, type 2 2019-05-28 criteria provided, single submitter clinical testing

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