ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1467_1479del (p.Asn490fs)

dbSNP: rs1580565026
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987558 SCV001136885 pathogenic Familial adenomatous polyposis 1 2019-05-28 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV001356693 SCV001551932 uncertain significance not provided no assertion criteria provided clinical testing

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