ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.3411T>C (p.Tyr1137=) (rs4986763)

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Total submissions: 10
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000755224 SCV000602886 benign not provided 2017-05-02 criteria provided, single submitter clinical testing
Ambry Genetics RCV000162378 SCV000212688 benign Hereditary cancer-predisposing syndrome 2014-11-11 criteria provided, single submitter clinical testing
Color RCV000162378 SCV000537323 benign Hereditary cancer-predisposing syndrome 2015-03-31 criteria provided, single submitter clinical testing
Counsyl RCV000410144 SCV000489873 benign Fanconi anemia, complementation group J 2016-06-18 criteria provided, single submitter clinical testing
Counsyl RCV000411217 SCV000489874 benign Neoplasm of ovary 2016-06-18 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000283962 SCV000404572 likely benign Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000341269 SCV000404573 likely benign Neoplasm of the breast 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000549583 SCV000633672 benign Familial cancer of breast; Fanconi anemia, complementation group J 2017-07-10 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000251677 SCV000538505 benign not specified 2016-03-29 criteria provided, single submitter clinical testing Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency
PreventionGenetics RCV000251677 SCV000314840 benign not specified criteria provided, single submitter clinical testing

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