ClinVar Miner

Submissions for variant NM_000038.6(APC):c.3552C>T (p.Ala1184=) (rs759407858)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000229596 SCV000282744 likely benign Familial adenomatous polyposis 1 2017-09-21 criteria provided, single submitter clinical testing
Counsyl RCV000229596 SCV000489563 likely benign Familial adenomatous polyposis 1 2016-10-28 criteria provided, single submitter clinical testing
Ambry Genetics RCV000575208 SCV000667344 likely benign Hereditary cancer-predisposing syndrome 2015-05-29 criteria provided, single submitter clinical testing
Color RCV000575208 SCV000681614 likely benign Hereditary cancer-predisposing syndrome 2017-04-20 criteria provided, single submitter clinical testing

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