ClinVar Miner

Submissions for variant NM_004329.2(BMPR1A):c.765C>T (p.Gly255=) (rs786201114)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000162690 SCV000213144 likely benign Hereditary cancer-predisposing syndrome 2016-02-05 criteria provided, single submitter clinical testing
Invitae RCV000758779 SCV000562741 likely benign not provided 2019-02-15 criteria provided, single submitter clinical testing
Color RCV000162690 SCV000682917 likely benign Hereditary cancer-predisposing syndrome 2016-03-21 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000758779 SCV000887611 likely benign not provided 2018-08-01 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000758779 SCV001150629 likely benign not provided 2018-06-01 criteria provided, single submitter clinical testing

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