ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4185+11TG[7]

dbSNP: rs273900723
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000410509 SCV000488296 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 1 2016-02-17 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000583895 SCV000688474 likely benign Hereditary cancer-predisposing syndrome 2022-10-13 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA1) RCV000410509 SCV000145012 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 1 2010-12-17 no assertion criteria provided clinical testing
BRCAlab, Lund University RCV000410509 SCV004244000 likely benign Breast-ovarian cancer, familial, susceptibility to, 1 2024-01-17 no assertion criteria provided clinical testing

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