ClinVar Miner

Submissions for variant NM_000038.6(APC):c.7604G>A (p.Ser2535Asn)

dbSNP: rs1355563057
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000581290 SCV000687135 uncertain significance Hereditary cancer-predisposing syndrome 2019-03-25 criteria provided, single submitter clinical testing
Mendelics RCV000987584 SCV001136945 uncertain significance Familial adenomatous polyposis 1 2019-05-28 criteria provided, single submitter clinical testing

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