ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.6915G>A (p.Lys2305=) (rs1555285156)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000587051 SCV000695005 likely benign not specified 2019-08-21 criteria provided, single submitter clinical testing
Invitae RCV000929536 SCV001075169 likely benign not provided 2018-09-27 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000929536 SCV001133880 uncertain significance not provided 2018-10-18 criteria provided, single submitter clinical testing
Ambry Genetics RCV001025798 SCV001188056 likely benign Hereditary cancer-predisposing syndrome 2018-09-07 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Color Health, Inc RCV001025798 SCV001345633 likely benign Hereditary cancer-predisposing syndrome 2019-02-28 criteria provided, single submitter clinical testing
Invitae RCV001448843 SCV001651946 likely benign Hereditary breast and ovarian cancer syndrome 2018-09-20 criteria provided, single submitter clinical testing

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