ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.1935+11_1935+13delGTT (rs730881641)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000160353 SCV000684167 benign Hereditary cancer-predisposing syndrome 2016-04-19 criteria provided, single submitter clinical testing
Counsyl RCV000409823 SCV000489821 likely benign Fanconi anemia, complementation group J 2016-06-03 criteria provided, single submitter clinical testing
Counsyl RCV000410417 SCV000489822 likely benign Neoplasm of ovary 2016-06-03 criteria provided, single submitter clinical testing
GeneDx RCV000160353 SCV000210859 benign Hereditary cancer-predisposing syndrome 2014-07-01 criteria provided, single submitter clinical testing The variant is found in HEREDICANCER panel(s).
Illumina Clinical Services Laboratory,Illumina RCV000357839 SCV000404602 uncertain significance Neoplasm of the breast 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000265496 SCV000404603 uncertain significance Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing

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