ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8691T>G (p.Ala2897=)

dbSNP: rs1283898827
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759676 SCV000889160 uncertain significance not provided 2018-01-19 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001192236 SCV001360263 likely benign Hereditary cancer-predisposing syndrome 2019-01-23 criteria provided, single submitter clinical testing

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