ClinVar Miner

Submissions for variant NM_001128425.1(MUTYH):c.1014G>T (p.Gln338His) (rs3219489)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000640420 SCV000762011 likely benign MYH-associated polyposis 2017-12-06 criteria provided, single submitter clinical testing
Color Health, Inc RCV000777602 SCV000913468 uncertain significance Hereditary cancer-predisposing syndrome 2019-01-16 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000584255 SCV000691948 benign not specified no assertion criteria provided clinical testing

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