ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.3963C>G (p.Ser1321=) (rs1567789440)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759531 SCV000888905 uncertain significance not provided 2018-08-22 criteria provided, single submitter clinical testing
Invitae RCV000759531 SCV001087081 likely benign not provided 2018-08-10 criteria provided, single submitter clinical testing
Invitae RCV001399337 SCV001601125 likely benign Hereditary breast and ovarian cancer syndrome 2018-08-09 criteria provided, single submitter clinical testing

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